Data Coordinator
Care Access · United States · US
Clinical Research
Remote
Dentist
Demand78
Career growth68
Healthcare fit82
Remote potential50
Salary band
USD 26 – 36
5-year outlook
Likely a stable entry-to-mid clinical research operations role with modest salary growth; experienced coordinators can progress toward clinical research associate, data management, or site coordination roles, but exact pay depends on location and employer.
Clinical license
Not required
Applicant reach
broad
Seniority
entry
Employment type
full-time
Date found
2026-10-25
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- License jurisdiction
- US
- Profession fit
- Dentist
- Rate period
- Hourly
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
A practical entry point into clinical research for detail-oriented clinicians and healthcare graduates who want non-clinical experience in data quality, EDC systems, and trial operations. Less compelling for senior clinicians seeking strategy, leadership, or higher compensation immediately.
Who should apply
Nurses, pharmacists, allied health professionals, IMGs, and healthcare graduates seeking to enter clinical research operations; doctors exploring non-clinical trial support roles may also apply but should expect an entry-level data-focused position.
CV angle
Frame real clinical experience around documentation accuracy, source record review, protocol adherence, adverse event and informed consent tracking, data reconciliation, and attention to detail. Highlight any exposure to EDC/CRF systems, clinical audits, quality checks, or research study workflows without overstating responsibilities.
Skills to highlight
- Clinical research documentation
- Source data review and quality control
- EDC/CRF data entry
- Data reconciliation
- Query management and follow-up
- Protocol compliance
- Adverse event and informed consent tracking
- Attention to detail
Role summary
A centralized clinical research data coordination role focused on reviewing source records, entering trial data into sponsor EDC/CRF systems, reconciling visit documentation, managing queries, and helping keep study records accurate and inspection-ready.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.