Clinical Research Coordinator
SOC 11-9121.01 · ESCO 2212 · OSCA 224931
Role snapshot
Overview
Manages the day-to-day operations of clinical trials, recruiting participants, obtaining informed consent, and ensuring study protocols are followed precisely. Collects and records patient data, coordinates with sponsors, and prepares regulatory submissions. This role is crucial for the ethical and efficient conduct of medical research, contributing directly to the development of new treatments and therapies.
Plays a vital role in advancing medical science by ensuring the integrity and safety of clinical trials, which are essential for bringing new medications and treatments to patients. Contributes to public health by meticulously collecting data that informs healthcare decisions.
On the job
- Recruit and screen potential study participants according to inclusion/exclusion criteria
- Obtain informed consent from participants and ensure ongoing understanding of the study
- Collect and record patient data accurately and completely, often using Electronic Data Capture (EDC) systems
- Ensure strict adherence to study protocols, Good Clinical Practice (GCP), and regulatory requirements
- Coordinate participant visits, perform study-related procedures (e.g., vital signs, ECGs, blood draws), and manage study drug accountability
- Communicate regularly with study sponsors, investigators, and institutional review boards (IRBs)
Tools & technology
Average salary
Job outlook
GrowingJob growth is expected to be above average over the next five years.
Education & training
Bachelor's degree in nursing, life sciences, or a related health field is typically required. Master's degree may be preferred for senior or specialized roles.
Career pathways
WHERE YOU COULD GO
CURRENT ROLE
Clinical Research Coordinator
Medical & Clinical
ADJACENT MOVES
STARTING POINTS
Who thrives here
Interest profile
investigative · ICE
Individuals who enjoy investigating complex problems, working with data and protocols, and coordinating efforts to achieve structured goals, often thrive in this role. The combination of investigative curiosity, conventional adherence to rules, and enterprising coordination skills is key.
Personality characteristics
Organized
Consistently follows strict protocols and manages detailed documentation to ensure accuracy and compliance in clinical trials.
Investigative
Possesses a keen interest in scientific inquiry and carefully analyzes data to identify trends or discrepancies in research.
Collaborative
Works effectively with study participants, investigators, sponsors, and other team members to achieve research objectives.
Proactive
Takes initiative in managing trial logistics, resolving issues, and ensuring timely progress of studies.
Composed
Maintains a calm and steady demeanor when facing challenges, unexpected issues, or strict deadlines in a regulated environment.
Best for
- Individuals who are highly organized, detail-oriented, and committed to scientific integrity.
- Professionals who enjoy a mix of patient interaction, data management, and regulatory oversight.
- Those looking for a career that directly contributes to medical research and public health.
Watch out for
- The highly structured and regulated nature of the work may not suit those who prefer less rigid environments or more creative freedom.
- Requires constant attention to detail and adherence to strict protocols, which can be demanding for some.
- Occasional weekend work may be required due to patient schedules or urgent study needs.
A week in the life
A representative working week for a Clinical Research Coordinator — where the deep work, meetings, and admin actually land.
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