A Clinical Research Coordinator begins their day reviewing study protocols and scheduling patient appointments for procedures or inpatient stays according to research timelines. They conduct eligibility assessments through screening interviews and medical record reviews, then perform protocol-specific procedures like taking vital signs, conducting electrocardiograms, and interviewing study subjects. Throughout the day, they maintain detailed case report forms, drug dispensation records, and regulatory documentation while monitoring compliance with local, federal, and state requirements. They spend considerable time communicating with patients and caregivers about study expectations, tracking enrollment status, and documenting any dropout information or protocol deviations. Their work involves coding and interpreting collected study data, identifying protocol problems, and coordinating with investigators to resolve issues that arise during the research process.
Individuals who excel as Clinical Research Coordinators demonstrate exceptional dependability and attention to detail, as evidenced by the highest importance ratings (9.0 and 8.0 respectively) for these work styles. They possess strong investigative tendencies (RIASEC I:5.90) combined with conventional organizational skills (C:4.81), enabling them to systematically approach complex research protocols while maintaining meticulous records. These professionals thrive on intellectual curiosity and cautiousness, balancing scientific rigor with participant safety concerns. The role suits those with excellent written and oral communication abilities (importance 4.0 each) who can effectively bridge technical research concepts with patient care, while managing multiple concurrent studies with precision and integrity.
Clinical Research Coordinators face moderate automation risk in data entry and basic documentation tasks, as Electronic Data Capture (EDC) systems and clinical trial management systems increasingly automate routine record-keeping functions. However, the core responsibilities requiring human judgment remain secure, including participant assessment, protocol interpretation, regulatory compliance monitoring, and the complex interpersonal communications essential to informed consent and patient care. The emphasis on critical thinking, problem sensitivity, and social perceptiveness in managing study participants and resolving protocol issues represents distinctly human capabilities that complement rather than compete with technological advances in clinical research infrastructure.
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| TERM | COUNT | FREQ | BAR | SOURCE ATTRIBUTION |
|---|---|---|---|---|
| clinical | 68 | 0.0175 | wikipedia 60% inference 37% | |
| research | 62 | 0.0159 | wikipedia 55% inference 35% | |
| others | 42 | 0.0108 | onet dimensi 90% dwas 7% | |
| tendency | 42 | 0.0108 | onet dimensi 100% | |
| study | 36 | 0.0092 | wikipedia 42% onet tasks 39% | |
| equipment | 30 | 0.0077 | onet dimensi 77% onet tasks 10% | |
| subject | 28 | 0.0072 | wikipedia 86% onet tasks 14% | |
| subjects | 24 | 0.0062 | wikipedia 62% onet tasks 21% | |
| procedures | 24 | 0.0062 | onet dimensi 33% wikipedia 29% | |
| activities | 21 | 0.0054 | onet dimensi 43% dwas 43% | |
| human | 20 | 0.0051 | wikipedia 50% onet dimensi 35% | |
| crc | 20 | 0.0051 | wikipedia 100% | |
| trial | 20 | 0.0051 | wikipedia 85% inference 15% | |
| medical | 19 | 0.0049 | wikipedia 53% dwas 16% | |
| principles | 18 | 0.0046 | onet dimensi 89% wikipedia 6% | |
| protocol | 17 | 0.0044 | wikipedia 41% onet tasks 29% | |
| regulatory | 15 | 0.0039 | inference 60% dwas 20% | |
| consent | 15 | 0.0039 | wikipedia 80% onet tasks 13% | |
| compliance | 14 | 0.0036 | inference 43% dwas 29% | |
| informed | 14 | 0.0036 | wikipedia 79% onet tasks 14% | |
| care | 14 | 0.0036 | wikipedia 50% onet tasks 21% | |
| management | 14 | 0.0036 | onet dimensi 50% inference 29% | |
| events | 14 | 0.0036 | onet dimensi 57% wikipedia 36% | |
| monitoring | 14 | 0.0036 | onet dimensi 57% wikipedia 29% | |
| problems | 13 | 0.0033 | onet dimensi 69% onet tasks 15% | |
| materials | 13 | 0.0033 | onet dimensi 77% dwas 15% | |
| patient | 13 | 0.0033 | wikipedia 69% inference 23% | |
| includes | 13 | 0.0033 | onet dimensi 92% wikipedia 8% | |
| irb | 13 | 0.0033 | wikipedia 100% | |
| trials | 12 | 0.0031 | wikipedia 75% inference 17% |
Provenance Window — Full Source Record · 11-9121.01 · Clinical Research Coordinators 7 source blocks · click to expand
[Core] [53% incumbents] Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols. DWAs: Schedule activities or facility use. [Core] [53% incumbents] Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms. DWAs: Interview employees, customers, or others to collect information. [Core] [53% incumbents] Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses. DWAs: Interview employees, customers, or others to collect information. [Core] [53% incumbents] Inform patients or caregivers about study aspects and outcomes to be expected. DWAs: Communicate organizational information to customers or other stakeholders. [Core] [53% incumbents] Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices. DWAs: Monitor organizational compliance with regulations. [Core] [53% incumbents] Oversee subject enrollment to ensure that informed consent is properly obtained and documented. DWAs: Monitor activities of individuals to ensure safety or compliance with rules. [Core] [53% incumbents] Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms. DWAs: Maintain regulatory or compliance documentation. [Core] [53% incumbents] Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions. DWAs: Analyze data to identify or resolve operational problems. [Core] [53% incumbents] Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts. DWAs: Maintain operational records. [Core] [53% incumbents] Code, evaluate, or interpret collected study data. DWAs: Interpret research or operational data. | Code data or other information. [Core] [53% incumbents] Direct the requisition, collection, labeling, storage, or shipment of specimens. DWAs: Manage operations, research, or logistics projects. [Core] [53% incumbents] Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures. DWAs: Conduct employee training programs. [Core] [53% incumbents] Order drugs or devices necessary for study completion. DWAs: Purchase materials, equipment, or other resources. [Core] [53% incumbents] Contact outside health care providers and communicate with subjects to obtain follow-up information. DWAs: Interview employees, customers, or others to collect information. | Coordinate with external parties to exchange information. [Core] [53% incumbents] Confer with health care professionals to determine the best recruitment practices for studies. DWAs: Confer with organizational members to accomplish work activities. [Core] [53% incumbents] Communicate with laboratories or investigators regarding laboratory findings. DWAs: Confer with organizational members to accomplish work activities. | Coordinate with external parties to exchange information. [Core] [53% incumbents] Organize space for study equipment and supplies. DWAs: Plan facility layouts or designs. [Core] [53% incumbents] Develop advertising and other informational materials to be used in subject recruitment. DWAs: Develop promotional materials. [Supplemental] [53% incumbents] Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics. DWAs: Advise customers on technical or procedural issues. [Supplemental] [53% incumbents] Contact industry representatives to ensure equipment and software specifications necessary for successful study completion. DWAs: Coordinate operational activities with external stakeholders. [Supplemental] [53% incumbents] Register protocol patients with appropriate statistical centers as required. DWAs: Perform clerical work in medical settings. [Supplemental] [53% incumbents] Solicit industry-sponsored trials through contacts and professional organizations. DWAs: Promote products, services, or programs. [Supplemental] [53% incumbents] Participate in preparation and management of research budgets and monetary disbursements. DWAs: Manage organizational or project budgets. [Core] [52% incumbents] Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports. DWAs: Prepare operational progress or status reports. [Core] [52% incumbents] Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies. DWAs: Maintain regulatory or compliance documentation. | Communicate with government agencies. [Core] [52% incumbents] Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks. DWAs: Analyze risks to minimize losses or damages. [Core] [52% incumbents] Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions. DWAs: Coordinate operational activities with external stakeholders. [Core] [52% incumbents] Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data. DWAs: Coordinate operational activities with external stakeholders. [Core] [52% incumbents] Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. DWAs: Conduct financial or regulatory audits. [Core] [52% incumbents] Participate in the development of study protocols including guidelines for administration or data collection procedures. DWAs: Develop organizational methods or procedures. [Core] [52% incumbents] Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues. DWAs: Maintain knowledge of current developments in area of expertise. [Supplemental] [52% incumbents] Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary. DWAs: Calculate numerical data for medical activities. | Prepare medications or medical solutions. | Instruct patients in the use of assistive equipment. [Supplemental] [52% incumbents] Arrange for research study sites and determine staff or equipment availability. DWAs: Schedule activities or facility use.
--- SKILLS --- Reading Comprehension (imp:4.00 lvl:4.25) — Understanding written sentences and paragraphs in work-related documents. Active Listening (imp:4.00 lvl:4.00) — Giving full attention to what other people are saying, taking time to understand Writing (imp:4.00 lvl:4.00) — Communicating effectively in writing as appropriate for the needs of the audienc Speaking (imp:3.88 lvl:4.00) — Talking to others to convey information effectively. Critical Thinking (imp:3.75 lvl:4.00) — Using logic and reasoning to identify the strengths and weaknesses of alternativ Monitoring (imp:3.62 lvl:3.75) — Monitoring/Assessing performance of yourself, other individuals, or organization Active Learning (imp:3.38 lvl:4.00) — Understanding the implications of new information for both current and future pr Learning Strategies (imp:3.12 lvl:3.38) — Selecting and using training/instructional methods and procedures appropriate fo Science (imp:3.00 lvl:3.00) — Using scientific rules and methods to solve problems. Mathematics (imp:2.88 lvl:3.00) — Using mathematics to solve problems. --- KNOWLEDGE --- Customer and Personal Service (imp:4.27 lvl:4.85) — Knowledge of principles and processes for providing customer and personal servic English Language (imp:3.77 lvl:4.07) — Knowledge of the structure and content of the English language including the mea Administrative (imp:3.73 lvl:4.38) — Knowledge of administrative and office procedures and systems such as word proce Medicine and Dentistry (imp:3.24 lvl:3.07) — Knowledge of the information and techniques needed to diagnose and treat human i Administration and Management (imp:2.97 lvl:2.84) — Knowledge of business and management principles involved in strategic planning, Biology (imp:2.96 lvl:3.15) — Knowledge of plant and animal organisms, their tissues, cells, functions, interd Computers and Electronics (imp:2.91 lvl:3.47) — Knowledge of circuit boards, processors, chips, electronic equipment, and comput Mathematics (imp:2.87 lvl:3.07) — Knowledge of arithmetic, algebra, geometry, calculus, statistics, and their appl Education and Training (imp:2.69 lvl:2.95) — Knowledge of principles and methods for curriculum and training design, teaching Public Safety and Security (imp:2.66 lvl:2.28) — Knowledge of relevant equipment, policies, procedures, and strategies to promote Personnel and Human Resources (imp:2.58 lvl:2.35) — Knowledge of principles and procedures for personnel recruitment, selection, tra Psychology (imp:2.58 lvl:2.95) — Knowledge of human behavior and performance; individual differences in ability, Chemistry (imp:2.51 lvl:2.51) — Knowledge of the chemical composition, structure, and properties of substances a Law and Government (imp:2.44 lvl:2.14) — Knowledge of laws, legal codes, court procedures, precedents, government regulat Sociology and Anthropology (imp:2.32 lvl:2.26) — Knowledge of group behavior and dynamics, societal trends and influences, human Communications and Media (imp:2.16 lvl:2.06) — Knowledge of media production, communication, and dissemination techniques and m Philosophy and Theology (imp:2.14 lvl:1.90) — Knowledge of different philosophical systems and religions. This includes their Therapy and Counseling (imp:2.06 lvl:1.64) — Knowledge of principles, methods, and procedures for diagnosis, treatment, and r Sales and Marketing (imp:2.02 lvl:1.87) — Knowledge of principles and methods for showing, promoting, and selling products Transportation (imp:2.00 lvl:1.75) — Knowledge of principles and methods for moving people or goods by air, rail, sea Telecommunications (imp:1.87 lvl:0.84) — Knowledge of transmission, broadcasting, switching, control, and operation of te Engineering and Technology (imp:1.81 lvl:1.38) — Knowledge of the practical application of engineering science and technology. Th Production and Processing (imp:1.77 lvl:1.18) — Knowledge of raw materials, production processes, quality control, costs, and ot Physics (imp:1.69 lvl:1.25) — Knowledge and prediction of physical principles, laws, their interrelationships, Economics and Accounting (imp:1.63 lvl:1.14) — Knowledge of economic and accounting principles and practices, the financial mar Geography (imp:1.58 lvl:1.07) — Knowledge of principles and methods for describing the features of land, sea, an Design (imp:1.50 lvl:0.91) — Knowledge of design techniques, tools, and principles involved in production of Mechanical (imp:1.42 lvl:0.79) — Knowledge of machines and tools, including their designs, uses, repair, and main History and Archeology (imp:1.37 lvl:0.56) — Knowledge of historical events and their causes, indicators, and effects on civi Foreign Language (imp:1.33 lvl:0.44) — Knowledge of the structure and content of a foreign (non-English) language inclu Fine Arts (imp:1.21) — Knowledge of the theory and techniques required to compose, produce, and perform Food Production (imp:1.07) — Knowledge of techniques and equipment for planting, growing, and harvesting food Building and Construction (imp:1.00) — Knowledge of materials, methods, and the tools involved in the construction or r --- ABILITIES --- Oral Comprehension (imp:4.00 lvl:4.38) — The ability to listen to and understand information and ideas presented through Written Comprehension (imp:4.00 lvl:4.25) — The ability to read and understand information and ideas presented in writing. Oral Expression (imp:4.00 lvl:4.25) — The ability to communicate information and ideas in speaking so others will unde Written Expression (imp:4.00 lvl:4.00) — The ability to communicate information and ideas in writing so others will under Problem Sensitivity (imp:4.00 lvl:4.00) — The ability to tell when something is wrong or is likely to go wrong. It does no Deductive Reasoning (imp:4.00 lvl:4.00) — The ability to apply general rules to specific problems to produce answers that Inductive Reasoning (imp:3.88 lvl:3.88) — The ability to combine pieces of information to form general rules or conclusion Information Ordering (imp:3.88 lvl:4.00) — The ability to arrange things or actions in a certain order or pattern according Speech Recognition (imp:3.75 lvl:3.75) — The ability to identify and understand the speech of another person. Speech Clarity (imp:3.75 lvl:3.75) — The ability to speak clearly so others can understand you. Near Vision (imp:3.62 lvl:3.62) — The ability to see details at close range (within a few feet of the observer). Category Flexibility (imp:3.25 lvl:3.50) — The ability to generate or use different sets of rules for combining or grouping Fluency of Ideas (imp:3.00 lvl:3.00) — The ability to come up with a number of ideas about a topic (the number of ideas Mathematical Reasoning (imp:3.00 lvl:3.00) — The ability to choose the right mathematical methods or formulas to solve a prob Number Facility (imp:3.00 lvl:3.00) — The ability to add, subtract, multiply, or divide quickly and correctly. Flexibility of Closure (imp:3.00 lvl:3.00) — The ability to identify or detect a known pattern (a figure, object, word, or so Perceptual Speed (imp:3.00 lvl:2.88) — The ability to quickly and accurately compare similarities and differences among Far Vision (imp:3.00 lvl:3.00) — The ability to see details at a distance. Originality (imp:2.88 lvl:3.00) — The ability to come up with unusual or clever ideas about a given topic or situa Speed of Closure (imp:2.88 lvl:3.00) — The ability to quickly make sense of, combine, and organize information into mea Selective Attention (imp:2.88 lvl:2.88) — The ability to concentrate on a task over a period of time without being distrac Time Sharing (imp:2.88 lvl:2.88) — The ability to shift back and forth between two or more activities or sources of Memorization (imp:2.62 lvl:2.88) — The ability to remember information such as words, numbers, pictures, and proced Visualization (imp:2.62 lvl:2.88) — The ability to imagine how something will look after it is moved around or when Visual Color Discrimination (imp:2.38 lvl:2.12) — The ability to match or detect differences between colors, including shades of c Auditory Attention (imp:2.38 lvl:1.88) — The ability to focus on a single source of sound in the presence of other distra Finger Dexterity (imp:2.00 lvl:1.75) — The ability to make precisely coordinated movements of the fingers of one or bot Hearing Sensitivity (imp:2.00 lvl:1.75) — The ability to detect or tell the differences between sounds that vary in pitch Depth Perception (imp:1.75 lvl:0.75) — The ability to judge which of several objects is closer or farther away from you Trunk Strength (imp:1.62 lvl:1.12) — The ability to use your abdominal and lower back muscles to support part of the Wrist-Finger Speed (imp:1.50 lvl:0.75) — The ability to make fast, simple, repeated movements of the fingers, hands, and Dynamic Strength (imp:1.25 lvl:0.25) — The ability to exert muscle force repeatedly or continuously over time. This inv Spatial Orientation (imp:1.12 lvl:0.12) — The ability to know your location in relation to the environment or to know wher Extent Flexibility (imp:1.12 lvl:0.12) — The ability to bend, stretch, twist, or reach with your body, arms, and/or legs. Arm-Hand Steadiness (imp:1.00) — The ability to keep your hand and arm steady while moving your arm or while hold Manual Dexterity (imp:1.00) — The ability to quickly move your hand, your hand together with your arm, or your Control Precision (imp:1.00) — The ability to quickly and repeatedly adjust the controls of a machine or a vehi Multilimb Coordination (imp:1.00) — The ability to coordinate two or more limbs (for example, two arms, two legs, or Response Orientation (imp:1.00) — The ability to choose quickly between two or more movements in response to two o Rate Control (imp:1.00) — The ability to time your movements or the movement of a piece of equipment in an Reaction Time (imp:1.00) — The ability to quickly respond (with the hand, finger, or foot) to a signal (sou Speed of Limb Movement (imp:1.00) — The ability to quickly move the arms and legs. Static Strength (imp:1.00) — The ability to exert maximum muscle force to lift, push, pull, or carry objects. Explosive Strength (imp:1.00) — The ability to use short bursts of muscle force to propel oneself (as in jumping Stamina (imp:1.00) — The ability to exert yourself physically over long periods of time without getti Dynamic Flexibility (imp:1.00) — The ability to quickly and repeatedly bend, stretch, twist, or reach out with yo Gross Body Coordination (imp:1.00) — The ability to coordinate the movement of your arms, legs, and torso together wh Gross Body Equilibrium (imp:1.00) — The ability to keep or regain your body balance or stay upright when in an unsta Night Vision (imp:1.00) — The ability to see under low-light conditions. Peripheral Vision (imp:1.00) — The ability to see objects or movement of objects to one's side when the eyes ar Glare Sensitivity (imp:1.00) — The ability to see objects in the presence of a glare or bright lighting. Sound Localization (imp:1.00) — The ability to tell the direction from which a sound originated. --- WORK ACTIVITIES --- Documenting/Recording Information (imp:4.53 lvl:4.52) — Entering, transcribing, recording, storing, or maintaining information in writte Organizing, Planning, and Prioritizing Work (imp:4.43 lvl:5.79) — Developing specific goals and plans to prioritize, organize, and accomplish your Getting Information (imp:4.39 lvl:4.80) — Observing, receiving, and otherwise obtaining information from all relevant sour Working with Computers (imp:4.39 lvl:3.83) — Using computers and computer systems (including hardware and software) to progra Communicating with Supervisors, Peers, or Subordinates (imp:4.13 lvl:4.67) — Providing information to supervisors, co-workers, and subordinates by telephone, Monitoring Processes, Materials, or Surroundings (imp:4.10 lvl:5.20) — Monitoring and reviewing information from materials, events, or the environment, Evaluating Information to Determine Compliance with Standards (imp:4.08 lvl:4.52) — Using relevant information and individual judgment to determine whether events o Scheduling Work and Activities (imp:4.01 lvl:4.22) — Scheduling events, programs, and activities, as well as the work of others. Performing Administrative Activities (imp:3.94 lvl:4.11) — Performing day-to-day administrative tasks such as maintaining information files Establishing and Maintaining Interpersonal Relationships (imp:3.86 lvl:5.17) — Developing constructive and cooperative working relationships with others, and m Identifying Objects, Actions, and Events (imp:3.74 lvl:4.53) — Identifying information by categorizing, estimating, recognizing differences or Making Decisions and Solving Problems (imp:3.70 lvl:4.36) — Analyzing information and evaluating results to choose the best solution and sol Training and Teaching Others (imp:3.54 lvl:3.58) — Identifying the educational needs of others, developing formal educational or tr Processing Information (imp:3.48 lvl:4.71) — Compiling, coding, categorizing, calculating, tabulating, auditing, or verifying Assisting and Caring for Others (imp:3.48 lvl:4.05) — Providing personal assistance, medical attention, emotional support, or other pe Analyzing Data or Information (imp:3.45 lvl:4.28) — Identifying the underlying principles, reasons, or facts of information by break Updating and Using Relevant Knowledge (imp:3.41 lvl:4.13) — Keeping up-to-date technically and applying new knowledge to your job. Coordinating the Work and Activities of Others (imp:3.23 lvl:3.78) — Getting members of a group to work together to accomplish tasks. Performing for or Working Directly with the Public (imp:3.20 lvl:3.43) — Performing for people or dealing directly with the public. This includes serving Judging the Qualities of Objects, Services, or People (imp:3.18 lvl:3.51) — Assessing the value, importance, or quality of things or people. Thinking Creatively (imp:3.13 lvl:3.54) — Developing, designing, or creating new applications, ideas, relationships, syste Communicating with People Outside the Organization (imp:3.13 lvl:3.74) — Communicating with people outside the organization, representing the organizatio Interpreting the Meaning of Information for Others (imp:3.12 lvl:2.66) — Translating or explaining what information means and how it can be used. Coaching and Developing Others (imp:3.00 lvl:3.39) — Identifying the developmental needs of others and coaching, mentoring, or otherw Inspecting Equipment, Structures, or Materials (imp:2.98 lvl:3.39) — Inspecting equipment, structures, or materials to identify the cause of errors o Developing Objectives and Strategies (imp:2.87 lvl:2.86) — Establishing long-range objectives and specifying the strategies and actions to Estimating the Quantifiable Characteristics of Products, Events, or Information (imp:2.79 lvl:2.94) — Estimating sizes, distances, and quantities; or determining time, costs, resourc Monitoring and Controlling Resources (imp:2.73 lvl:3.14) — Monitoring and controlling resources and overseeing the spending of money. Developing and Building Teams (imp:2.67 lvl:2.38) — Encouraging and building mutual trust, respect, and cooperation among team membe Performing General Physical Activities (imp:2.49 lvl:2.38) — Performing general physical activities includes doing activities that require co Handling and Moving Objects (imp:2.45 lvl:2.90) — Using hands and arms in handling, installing, positioning, and moving materials, Resolving Conflicts and Negotiating with Others (imp:2.43 lvl:2.58) — Handling complaints, settling disputes, and resolving grievances and conflicts, Providing Consultation and Advice to Others (imp:2.36 lvl:3.42) — Providing guidance and expert advice to management or other groups on technical, Guiding, Directing, and Motivating Subordinates (imp:2.26 lvl:2.44) — Providing guidance and direction to subordinates, including setting performance Controlling Machines and Processes (imp:2.16 lvl:2.15) — Using either control mechanisms or direct physical activity to operate machines Repairing and Maintaining Electronic Equipment (imp:1.96 lvl:1.60) — Servicing, repairing, calibrating, regulating, fine-tuning, or testing machines, Drafting, Laying Out, and Specifying Technical Devices, Parts, and Equipment (imp:1.94 lvl:1.75) — Providing documentation, detailed instructions, drawings, or specifications to t Repairing and Maintaining Mechanical Equipment (imp:1.81 lvl:1.43) — Servicing, repairing, adjusting, and testing machines, devices, moving parts, an Selling or Influencing Others (imp:1.60 lvl:1.07) — Convincing others to buy merchandise/goods or to otherwise change their minds or Staffing Organizational Units (imp:1.57 lvl:1.14) — Recruiting, interviewing, selecting, hiring, and promoting employees in an organ Operating Vehicles, Mechanized Devices, or Equipment (imp:1.40) — Running, maneuvering, navigating, or driving vehicles or mechanized equipment, s --- WORK STYLES --- Dependability (imp:9.00) — A tendency to be reliable, responsible, and consistent in meeting work-related o Attention to Detail (imp:8.00) — A tendency to be detail-oriented, organized, and thorough in completing work. Integrity (imp:7.00) — A tendency to be honest and ethical at work. Cautiousness (imp:6.00) — A tendency to be careful, deliberate, and risk-avoidant when making work-related Intellectual Curiosity (imp:5.00) — A tendency to seek out and acquire new work-related knowledge and obtain a deep Cooperation (imp:4.00) — A tendency to be pleasant, helpful, and willing to assist others at work. Achievement Orientation (imp:3.00) — A tendency to establish and maintain personally challenging work-related goals, Attention to Detail (imp:2.77) — A tendency to be detail-oriented, organized, and thorough in completing work. Dependability (imp:2.65) — A tendency to be reliable, responsible, and consistent in meeting work-related o Integrity (imp:2.40) — A tendency to be honest and ethical at work. Cautiousness (imp:2.35) — A tendency to be careful, deliberate, and risk-avoidant when making work-related Cooperation (imp:2.34) — A tendency to be pleasant, helpful, and willing to assist others at work. Intellectual Curiosity (imp:2.12) — A tendency to seek out and acquire new work-related knowledge and obtain a deep Achievement Orientation (imp:2.11) — A tendency to establish and maintain personally challenging work-related goals, Adaptability (imp:2.09) — A tendency to be open to and comfortable with change, new experiences, or ideas Perseverance (imp:2.01) — A tendency to exhibit determination and resolve to perform or complete tasks in Perseverance (imp:2.00) — A tendency to exhibit determination and resolve to perform or complete tasks in Stress Tolerance (imp:1.99) — A tendency to cope and function effectively in stressful situations at work. Social Orientation (imp:1.79) — A tendency to seek out, enjoy, and be energized by social interaction at work. Leadership Orientation (imp:1.78) — A tendency to lead, take charge, offer opinions, and provide direction at work. Empathy (imp:1.77) — A tendency to show concern for others and be sensitive to others' needs and feel Sincerity (imp:1.75) — A tendency to be genuine and sincere in interactions with others at work, withou Self-Control (imp:1.70) — A tendency to remain calm and composed and to manage emotions effectively in res Tolerance for Ambiguity (imp:1.58) — A tendency to be comfortable with ambiguity and uncertainty at work. Self-Confidence (imp:1.57) — A tendency to believe in one's work-related capabilities and ability to control Initiative (imp:1.53) — A tendency to be proactive and take on extra responsibilities and tasks that may Innovation (imp:1.23) — A tendency to be inventive, to be imaginative, and to adopt new perspectives on Humility (imp:1.12) — A tendency to be modest and humble when interacting with others at work. Optimism (imp:1.04) — A tendency to exhibit a positive attitude and positive emotions at work, even un Adaptability (imp:1.00) — A tendency to be open to and comfortable with change, new experiences, or ideas Innovation () — A tendency to be inventive, to be imaginative, and to adopt new perspectives on Tolerance for Ambiguity () — A tendency to be comfortable with ambiguity and uncertainty at work. Initiative () — A tendency to be proactive and take on extra responsibilities and tasks that may Self-Confidence () — A tendency to believe in one's work-related capabilities and ability to control Leadership Orientation () — A tendency to lead, take charge, offer opinions, and provide direction at work. Humility () — A tendency to be modest and humble when interacting with others at work. Sincerity () — A tendency to be genuine and sincere in interactions with others at work, withou Empathy () — A tendency to show concern for others and be sensitive to others' needs and feel Optimism () — A tendency to exhibit a positive attitude and positive emotions at work, even un Social Orientation () — A tendency to seek out, enjoy, and be energized by social interaction at work. Stress Tolerance () — A tendency to cope and function effectively in stressful situations at work. Self-Control () — A tendency to remain calm and composed and to manage emotions effectively in res --- TRANSFERABLE SKILLS --- Coordination (imp:3.88 lvl:4.12) — Adjusting actions in relation to others' actions. Social Perceptiveness (imp:3.62 lvl:3.75) — Being aware of others' reactions and understanding why they react as they do. Complex Problem Solving (imp:3.62 lvl:3.62) — Identifying complex problems and reviewing related information to develop and ev Judgment and Decision Making (imp:3.62 lvl:3.62) — Considering the relative costs and benefits of potential actions to choose the m Time Management (imp:3.50 lvl:3.62) — Managing one's own time and the time of others. Management of Personnel Resources (imp:3.50 lvl:3.50) — Motivating, developing, and directing people as they work, identifying the best Instructing (imp:3.12 lvl:3.00) — Teaching others how to do something. Persuasion (imp:3.00 lvl:3.25) — Persuading others to change their minds or behavior. Service Orientation (imp:3.00 lvl:3.75) — Actively looking for ways to help people. Negotiation (imp:2.88 lvl:3.38) — Bringing others together and trying to reconcile differences. Systems Analysis (imp:2.88 lvl:2.88) — Determining how a system should work and how changes in conditions, operations, Systems Evaluation (imp:2.88 lvl:3.38) — Identifying measures or indicators of system performance and the actions needed Management of Material Resources (imp:2.75 lvl:2.75) — Obtaining and seeing to the appropriate use of equipment, facilities, and materi Management of Financial Resources (imp:2.38 lvl:2.25) — Determining how money will be spent to get the work done, and accounting for the Operations Monitoring (imp:1.75 lvl:1.25) — Watching gauges, dials, or other indicators to make sure a machine is working pr Quality Control Analysis (imp:1.75 lvl:1.12) — Conducting tests and inspections of products, services, or processes to evaluate Operations Analysis (imp:1.62 lvl:1.12) — Analyzing needs and product requirements to create a design. Technology Design (imp:1.62 lvl:0.75) — Generating or adapting equipment and technology to serve user needs. Programming (imp:1.62 lvl:0.88) — Writing computer programs for various purposes. Troubleshooting (imp:1.38 lvl:0.38) — Determining causes of operating errors and deciding what to do about it. Equipment Selection (imp:1.12 lvl:0.12) — Determining the kind of tools and equipment needed to do a job. Operation and Control (imp:1.12 lvl:0.12) — Controlling operations of equipment or systems. Installation (imp:1.00) — Installing equipment, machines, wiring, or programs to meet specifications. Equipment Maintenance (imp:1.00) — Performing routine maintenance on equipment and determining when and what kind o Repairing (imp:1.00) — Repairing machines or systems using the needed tools.
--- NATIONAL WAGES --- total_employment : 108,690 annual_median : $167,220 annual_pct10 : $79,710 annual_pct25 : $119,430 annual_pct75 : $221,540 annual_pct90 : $316,850 annual_mean : $180,250 hourly_median : $80.39 --- GEOGRAPHIC DISPERSION --- highest_state : Massachusetts ($267,290) lowest_state : Hawaii ($107,810) dispersion_ratio : 2.479x --- TOP STATES BY WAGE (49 total) --- Professional, Scientific, and Technical Services emp: 52,240 median: $ 202,000 Federal, State, and Local Government, excluding State and Local Government Schools and Hospitals and the U.S. Postal Service (OEWS Designation) emp: 19,320 median: $ 133,470 Manufacturing emp: 9,270 median: $ 185,110 Health Care and Social Assistance emp: 7,740 median: $ 99,980 Educational Services emp: 5,890 median: $ 82,060 Management of Companies and Enterprises emp: 5,080 median: $ 211,990 Wholesale Trade emp: 4,840 median: $ 216,890 Other Services (except Public Administration) emp: 1,370 median: $ 129,610 Administrative and Support and Waste Management and Remediation Services emp: 1,100 median: $ 111,240 Arts, Entertainment, and Recreation emp: 450 median: $ 103,480 --- TOP INDUSTRIES BY EMPLOYMENT (17 total) --- Professional, Scientific, and Technical Services emp: 52,240 median: $ 202,000 Federal, State, and Local Government, excluding State and Local Government Schools and Hospitals and the U.S. Postal Service (OEWS Designation) emp: 19,320 median: $ 133,470 Manufacturing emp: 9,270 median: $ 185,110 Health Care and Social Assistance emp: 7,740 median: $ 99,980 Educational Services emp: 5,890 median: $ 82,060 Management of Companies and Enterprises emp: 5,080 median: $ 211,990 Wholesale Trade emp: 4,840 median: $ 216,890 Other Services (except Public Administration) emp: 1,370 median: $ 129,610 Administrative and Support and Waste Management and Remediation Services emp: 1,100 median: $ 111,240 Arts, Entertainment, and Recreation emp: 450 median: $ 103,480
exact_match_status : found matched_title : Clinical research coordinator match_score : 0.9831 wikidata_qid : Q5133846 word_count : 1,584 wikipedia_url : https://en.wikipedia.org/wiki/Clinical_research_coordinator license : CC BY-SA 4.0 fetched_at : 2026-06-02T20:04:41.820623Z --- WIKIPEDIA FULL TEXT --- A Clinical Research Coordinator (CRC) is a person responsible for conducting clinical trials using good clinical practice (GCP) under the auspices of a Principal Investigator (PI). Good clinical practices principles have been defined by Madelene Ottosen, RN, MSN, of The University of Texas Health Science Center at Houston as: Trials are conducted ethically, as defined by the Declaration of Helsinki, rigorously, as defined by the International Conference on Harmonisation Guidelines (ICH). Benefits outweigh risks for each patient. Rights, safety and well-being of patients prevail over science. All available non-clinical and clinical information on any investigational agent can support the trial as designed. All trials are scientifically sound and clearly described. All clinical trials have current Institutional Review Board approval. Medical decisions and care are the responsibility of qualified health care professionals, specifically physicians and, if applicable, dentists. Everyone involved in the clinical trial is qualified by training, education and experience. Informed consent is given freely by every participant. All study documentation is recorded, handled and stored to allow accurate reporting, interpretation and verification. Confidentiality of subjects is respected and protected. Investigational products maintain Good Manufacturing Practice in storage, manufacturing and handling. Systems to ensure quality are implemented in all aspects of the trial. The PI is responsible for the conduct of the trial, however, "CRCs are often involved in essential duties that have been traditionally performed by the PI, such as conducting the informed consent process and ensuring compliance with the protocol." The CRC's primary responsibility, as with all clinical research professionals, is the protection of human subjects, but the CRC has many other responsibilities. Although not inclusive, some of the CRC responsibilities include preparing the Institutional Review Board submission, writing the informed consent document, working with the institutional official in contract negotiations, developing a detailed cost analysis, negotiating the budget with the Sponsor (i.e., pharmaceutical company or granting agency), subject recruitment, patient care, adverse event reporting, preparing the case report form (CRF), submitting CRFs and other data to the Sponsor as necessary and study close-out. == Responsibilities == === Feasibility === A sponsor sends a feasibility questionnaire to the local research site. The Clinical Research Coordinator completes the form on behalf of the site to determine if the local site has the patient population, support staff, medical facilities, and equipment necessary to successfully carry out the study protocol. === Institutional Review Board submissions === All research involving human subjects must be approved by an Institutional Review Board (IRB). Each IRB has protocol submission requirements, which typically involve an IRB application and informed consent document. A study cannot begin without IRB approval. === Informed consent === The IRB must approve informed consent prior to study initiation, and often the CRC is liaison between the IRB and the sponsor. The sponsor sets informed consent requirements, as does the IRB. Each local IRB must review and approve the informed consent, but the CRC is responsible for communication between the IRB and the sponsor. §46.116 of the Code of Federal Regulations outlines the basic elements of informed consent as a: Statement that the study involves research, an explanation of research purpose, expected duration of subject's participation, description of procedures, and identification of any experimental procedures Description of any reasonably foreseeable risk or discomfort to the subject Description of any benefits to the subject or others that can reasonably be expected Disclosure of appropriate alternative procedures or courses of treatment, if any, that might be advantageous to the subject Statement that describes extent, if any, to which confidentiality subject identity is maintained Explanation (if more than minimal risk to test subject) as to any compensation, medical treatments available if injury occurs and, or where further information is available List of whom to contact for pertinent questions about the research and subjects' rights, and whom to contact in the event of a research-related injury to the subject Statement that participation is voluntary, refusal to participate involves no penalty or loss of benefits, and that the subject may discontinue participation at any time without penalty or loss of benefits ==== Additional elements ==== When appropriate, experimenters also tell each subject: That the particular treatment or procedure may involve unforeseeable risks to the subject (or to an embryo or fetus, if relevant) Circumstances under which investigator may end subject's participation without subject's consent Additional costs to the subject that may result from participation in the research Consequences of subject withdrawing from the research, and procedures for orderly termination of subject participation That significant new findings during the research that could affect the subject's willingness to continue participation will be provided to the subject The approximate number of subjects involved in the study === Contracting with pharmaceutical companies === The site conducting the clinical trial negotiates the clinical trial agreement (CTA) to conform to its policies and procedures. The resolution of many contractual issues requires coordination between the sponsor, the PI and the site, which is usually the responsibility of the CRC. The involvement of each party is essential to a successful CTA with mutually acceptable terms. The CTA should include terms for indemnification, confidentiality, publication, intellectual property, insurance, data safety and monitoring boards, subject injury, governing law and termination clauses. === Cost analysis and budget negotiations === To develop a cost analysis, the CRC reviews the protocol schema and determine which procedures are standard of care, versus research. Research charges are included in the budget—with personnel effort, site initiation costs, IRB fees throughout the life of the clinical trial, pharmacy costs, travel costs for the PI and CRC to attend investigator meetings, equipment, dedicated fax and computer lines, supplies, screen failures, subject stipends, subject travel costs, and any other items defined as a direct cost to the clinical trial. In addition, if the clinical trial is at an Academic Medical Center (AMC), an indirect cost rate applies to the direct study costs. The indirect rate is approximately 30% for pharmaceutical trials, and can be upwards of 50% for federal trials, depending on the AMC's federally negotiated indirect costs rate. === Subject recruitment === Prior to agreeing to conduct the clinical trial, the CRC (and the PI) determine if they have the appropriate patient population. The CRC is responsible for subject recruitment once the trial begins, or must establish the research team that recruits subjects. Viable subject recruitment must occur beforehand, as the clinical trial agreement stipulates the number of subjects the site must recruit. === Patient care === The CRC coordinates and conduct patient care visits and assures that all procedures comply with the protocol. The CRC interacts with the PI to assure the patient receives appropriate medical evaluation and care when needed and alerts the PI of any serious adverse events that occur during the study. === Adverse events === An adverse event is described as "any adverse change in health or "side-effect" that occurs in a person who participates in a clinical trial while the patient is receiving the treatment (study medication, application of the study device, etc.) or within a pre-specified period of --- SEMANTIC NEIGHBORS (5) --- Title: Human subject research (similarity: 0.3846) URL: https://en.wikipedia.org/wiki/Human_subject_research QID: Q1331083 Extract: Human subjects research is systematic, scientific investigation that can be either interventional or observational and involves human beings as research subjects, commonly known as test subjects. Human subjects research can be either medical (clinical) research or non-medical research. Systematic in Title: Clinical trial management system (similarity: 0.5161) URL: https://en.wikipedia.org/wiki/Clinical_trial_management_system QID: Q1101537 Extract: A Clinical Trial Management System (CTMS) is a software system used by biotechnology and pharmaceutical industries to manage clinical trials in clinical research. The system maintains and manages planning, performing and reporting functions, along with participant contact information, tracking deadl Title: Glossary of clinical research (similarity: 0.5763) URL: https://en.wikipedia.org/wiki/Glossary_of_clinical_research QID: Q5571774 Extract: A glossary of terms used in clinical research. Title: Cirie Fields (similarity: 0.1429) URL: https://en.wikipedia.org/wiki/Cirie_Fields QID: Q5121897 Extract: Cirie Tiffany Fields is an American reality television personality and nurse best known for competing on multiple seasons of Survivor. Fields holds the record for most appearances in the franchise. Title: Jordi Mollà (similarity: 0.2439) URL: https://en.wikipedia.org/wiki/Jordi_Moll%C3%A0 QID: Q939395 Extract: Jordi Mollà Perales is a Spanish actor, artist, writer, and filmmaker from Catalonia. He has been nominated three times for the Goya Award for Best Actor for The Lucky Star (1997), Second Skin (1999), and El cónsul de Sodoma (2009).
model_pass1 : claude-sonnet-4-20250514
model_pass2 : claude-haiku-4-5-20251001
inference_confidence : high
confidence_notes : Strong confidence supported by comprehensive O*NET data, exact Wikipedia match, detailed wage and employment statistics, and clear task descriptions that align with the established definition of Clinical Research Coordinators in healthcare settings.
inferred_at : 2026-06-03T12:44:37.522425+00:00
tokens_input : 4,580
tokens_output : 4,656
cost_usd : $0.052322
wikipedia_used : True
wikipedia_title : Clinical research coordinator
wikipedia_note : Wikipedia confirms the role's responsibility for conducting clinical trials using Good Clinical Practice under Principal Investigator supervision. The semantic neighbors highlight connections to clinical trial management systems and human subjects research, reinforcing the regulatory and systematic nature of this profession.
--- PROSE FIELDS ---
ROLE SUMMARY:
Clinical Research Coordinators plan, direct, and coordinate clinical research projects, ensuring compliance with protocols and regulatory standards while managing study participants and data collection. They serve as the operational backbone of clinical trials, bridging scientific objectives with administrative execution through meticulous documentation and participant management. These professionals evaluate and analyze clinical data while overseeing the day-to-day activities of clinical research teams to maintain study integrity and regulatory compliance.
DAY IN THE LIFE:
A Clinical Research Coordinator begins their day reviewing study protocols and scheduling patient appointments for procedures or inpatient stays according to research timelines. They conduct eligibility assessments through screening interviews and medical record reviews, then perform protocol-specific procedures like taking vital signs, conducting electrocardiograms, and interviewing study subjects. Throughout the day, they maintain detailed case report forms, drug dispensation records, and regulatory documentation while monitoring compliance with local, federal, and state requirements. They spend considerable time communicating with patients and caregivers about study expectations, tracking enrollment status, and documenting any dropout information or protocol deviations. Their work involves coding and interpreting collected study data, identifying protocol problems, and coordinating with investigators to resolve issues that arise during the research process.
WHO THRIVES:
Individuals who excel as Clinical Research Coordinators demonstrate exceptional dependability and attention to detail, as evidenced by the highest importance ratings (9.0 and 8.0 respectively) for these work styles. They possess strong investigative tendencies (RIASEC I:5.90) combined with conventional organizational skills (C:4.81), enabling them to systematically approach complex research protocols while maintaining meticulous records. These professionals thrive on intellectual curiosity and cautiousness, balancing scientific rigor with participant safety concerns. The role suits those with excellent written and oral communication abilities (importance 4.0 each) who can effectively bridge technical research concepts with patient care, while managing multiple concurrent studies with precision and integrity.
CAREER ENTRY:
Entry into this field typically requires a bachelor's degree (60.1% of practitioners), with many positions accepting candidates from diverse educational backgrounds including life sciences, nursing, or health administration. Post-secondary certificates in clinical research or related healthcare fields provide an alternative pathway (11.6% of professionals), particularly for those transitioning from other healthcare roles. Prior experience in healthcare settings, research environments, or regulatory compliance provides valuable foundation knowledge, though many employers offer on-the-job training in specific protocols and Good Clinical Practice (GCP) standards. Professional certification through organizations like the Association of Clinical Research Professionals can enhance career prospects and demonstrate competency in clinical research principles.
CAREER TRAJECTORY:
Clinical Research Coordinators often advance to senior coordinator positions, Clinical Research Managers, or Clinical Program Directors within pharmaceutical companies, contract research organizations, or academic medical centers. The comprehensive skill set in regulatory compliance, data management, and project coordination opens pathways to specialized roles such as Clinical Data Managers or Health Informatics Specialists. Many professionals leverage their experience to transition into clinical affairs, regulatory affairs, or research and development leadership positions, with some pursuing advanced degrees to become Medical Scientists or moving into consulting roles within the growing clinical research industry.
MARKET INTELLIGENCE:
Clinical Research Coordinators command strong compensation with a median annual salary of $167,220 according to BLS OEWS May 2025 data, reflecting the specialized knowledge and regulatory responsibility inherent in the role. The profession employs 108,690 individuals nationwide with significant geographic variation, ranging from $267,290 in Massachusetts to $107,810 in Hawaii (2.48x ratio), indicating higher compensation in biotech and pharmaceutical hubs. The largest employment concentration is in Professional, Scientific, and Technical Services (52,240 employed), followed by government positions (19,320 employed) and manufacturing (9,270 employed). Job Zone 4 classification indicates considerable preparation needed, reflecting the critical role these professionals play in ensuring clinical trial integrity and participant safety. The field benefits from robust demand driven by pharmaceutical development pipelines and increased emphasis on evidence-based medicine.
AUTOMATION OUTLOOK:
Clinical Research Coordinators face moderate automation risk in data entry and basic documentation tasks, as Electronic Data Capture (EDC) systems and clinical trial management systems increasingly automate routine record-keeping functions. However, the core responsibilities requiring human judgment remain secure, including participant assessment, protocol interpretation, regulatory compliance monitoring, and the complex interpersonal communications essential to informed consent and patient care. The emphasis on critical thinking, problem sensitivity, and social perceptiveness in managing study participants and resolving protocol issues represents distinctly human capabilities that complement rather than compete with technological advances in clinical research infrastructure.
--- REASONED EDGES ---
[task_similarity] Clinical Data Managers (15-2051.02) — confidence:high
reasoning: Both roles involve maintaining clinical study records, coding and evaluating study data, and ensuring regulatory compliance.
data: Documenting/Recording Information (imp:4.5)
data: Working with Computers (imp:4.4)
data: Evaluating Information compliance (imp:4.1)
[knowledge_overlap] Clinical Nurse Specialists (29-1141.04) — confidence:high
reasoning: Both require strong Medicine and Dentistry knowledge and Customer/Personal Service skills for patient interaction.
data: Medicine and Dentistry knowledge (imp:3.2)
data: Customer and Personal Service (imp:4.3)
data: Patient assessment tasks
[skill_overlap] Health Informatics Specialists (15-1211.01) — confidence:medium
reasoning: Both utilize computers and electronics knowledge extensively and focus on healthcare data management and analysis.
data: Computers and Electronics (imp:2.9)
data: Working with Computers (imp:4.4)
data: Data coding and interpretation tasks
[career_pathway] Medical and Health Services Managers (11-9111.00) — confidence:high
reasoning: Clinical Research Coordinators commonly advance to management roles overseeing clinical programs and research operations.
data: Administration and Management knowledge
data: Organizing, Planning, and Prioritizing Work (imp:4.4)
data: Job Zone 4 preparation level
[riasec_cluster] Medical Scientists, Except Epidemiologists (19-1042.00) — confidence:medium
reasoning: Both share strong Investigative orientation (I:5.90) and require scientific methodology and research protocol understanding.
data: Investigative RIASEC code dominance
data: Biology knowledge (imp:3.0)
data: Protocol procedures and data analysis tasks
[transferable_skill] Biostatisticians (15-2041.01) — confidence:medium
reasoning: Both roles require complex problem solving and data analysis capabilities for interpreting clinical study results.
data: Complex Problem Solving (imp:3.6)
data: Mathematics knowledge (imp:2.9)
data: Data coding and evaluation tasks
[knowledge_overlap] Health Specialties Teachers, Postsecondary (25-1071.00) — confidence:medium
reasoning: Both require deep Medicine and Dentistry knowledge and strong communication skills for education and patient interaction.
data: Medicine and Dentistry knowledge
data: Speaking (imp:3.9)
data: Patient education and communication tasks
--- NORMALIZER SIGNALS ---
match_keywords : ['clinical research coordinator', 'clinical trial coordinator', 'clinical coordinator', 'research coordinator', 'clinical study coordinator', 'clinical data coordinator', 'clinical trial manager', 'clinical research manager']
exclude_keywords : ['laboratory technician', 'medical assistant', 'data analyst', 'research assistant', 'nurse practitioner']
title_patterns : ['Clinical Research *', 'Clinical Trial *', 'Clinical Study *', 'Clinical Data *', 'Clinical Program *']
common_variations: ['CRC', 'clinical research coord', 'clinical coordinator', 'research study coordinator', 'protocol coordinator', 'clinical trial coord', 'clinical research associate', 'clinical study manager']
total_terms : 40 top_words : ['clinical', 'research', 'others', 'tendency', 'study', 'equipment', 'subject', 'subjects', 'procedures', 'activities', 'human', 'crc', 'trial', 'medical', 'principles', 'protocol', 'regulatory', 'consent', 'compliance', 'informed'] source_layers : onet_tasks | onet_dimensions | dwas | wikipedia | inference TERM COUNT FREQ DOMINANT SOURCE SOURCE BREAKDOWN ────────────────────────────────────────────────────────────────────────────────────────── clinical 68 0.01747 wikipedia wikipedia:60% inference:37% onet_tasks:3% research 62 0.01593 wikipedia wikipedia:55% inference:35% onet_tasks:5% others 42 0.01079 onet_dimensions onet_dimensions:90% dwas:7% wikipedia:2% tendency 42 0.01079 onet_dimensions onet_dimensions:100% study 36 0.00925 wikipedia wikipedia:42% onet_tasks:39% inference:19% equipment 30 0.00771 onet_dimensions onet_dimensions:77% onet_tasks:10% dwas:7% subject 28 0.00719 wikipedia wikipedia:86% onet_tasks:14% subjects 24 0.00617 wikipedia wikipedia:62% onet_tasks:21% onet_dimensions:8% procedures 24 0.00617 onet_dimensions onet_dimensions:33% wikipedia:29% onet_tasks:25% activities 21 0.00539 onet_dimensions onet_dimensions:43% dwas:43% onet_tasks:10% human 20 0.00514 wikipedia wikipedia:50% onet_dimensions:35% inference:15% crc 20 0.00514 wikipedia wikipedia:100% trial 20 0.00514 wikipedia wikipedia:85% inference:15% medical 19 0.00488 wikipedia wikipedia:53% dwas:16% inference:16% principles 18 0.00462 onet_dimensions onet_dimensions:89% wikipedia:6% inference:6% protocol 17 0.00437 wikipedia wikipedia:41% onet_tasks:29% inference:29% regulatory 15 0.00385 inference inference:60% dwas:20% onet_tasks:13% consent 15 0.00385 wikipedia wikipedia:80% onet_tasks:13% inference:7% compliance 14 0.00360 inference inference:43% dwas:29% wikipedia:14% informed 14 0.00360 wikipedia wikipedia:79% onet_tasks:14% inference:7% care 14 0.00360 wikipedia wikipedia:50% onet_tasks:21% onet_dimensions:14% management 14 0.00360 onet_dimensions onet_dimensions:50% inference:29% onet_tasks:14% events 14 0.00360 onet_dimensions onet_dimensions:57% wikipedia:36% onet_tasks:7% monitoring 14 0.00360 onet_dimensions onet_dimensions:57% wikipedia:29% inference:14% problems 13 0.00334 onet_dimensions onet_dimensions:69% onet_tasks:15% dwas:8% materials 13 0.00334 onet_dimensions onet_dimensions:77% dwas:15% onet_tasks:8% patient 13 0.00334 wikipedia wikipedia:69% inference:23% onet_tasks:8% includes 13 0.00334 onet_dimensions onet_dimensions:92% wikipedia:8% irb 13 0.00334 wikipedia wikipedia:100% trials 12 0.00308 wikipedia wikipedia:75% inference:17% onet_tasks:8% control 12 0.00308 onet_dimensions onet_dimensions:100% objects 12 0.00308 onet_dimensions onet_dimensions:100% sponsor 12 0.00308 wikipedia wikipedia:100% standards 11 0.00283 onet_dimensions onet_dimensions:73% inference:18% onet_tasks:9% professionals 11 0.00283 inference inference:55% wikipedia:36% onet_tasks:9% appropriate 11 0.00283 onet_dimensions onet_dimensions:45% wikipedia:36% onet_tasks:18% adverse 11 0.00283 wikipedia wikipedia:82% onet_tasks:18% resources 11 0.00283 onet_dimensions onet_dimensions:82% dwas:9% wikipedia:9% costs 11 0.00283 wikipedia wikipedia:64% onet_dimensions:36% ideas 11 0.00283 onet_dimensions onet_dimensions:100%