Clinical Trials Manager (CTM)
Photocure · United States · US
Clinical Research
Remote
Nurse
Demand78
Career growth72
Healthcare fit78
Remote potential95
5-year outlook
Likely competitive for experienced clinical operations professionals in diagnostics and device trials, with compensation supported by GCP, IVD, CRO oversight, and regulatory submission experience. Exact salary will vary by location, experience, and diagnostics/device background.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-27
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- United States
- Profession fit
- Nurse
- Rate period
- Annual
Why this was classified this way
- contract
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
Worth applying if you have clinical research operations, CRO/vendor oversight, site monitoring, or diagnostics/device trial experience. It is less suitable for clinicians without prior trial management exposure because the role expects an experienced clinical operations professional.
Who should apply
Research nurses, clinical research coordinators ready to step up, physician-scientists or pharmacists with GCP and site/CRO experience, diagnostics or medical device clinical operations professionals, and clinicians with biomarker/IVD study exposure.
CV angle
Reframe real clinical and research experience around trial operations: GCP compliance, protocol/ICF/eCRF contributions, site coordination, IRB/ethics submissions, monitoring support, data query resolution, TMF maintenance, CAPA involvement, vendor/CRO collaboration, budget/timeline tracking, and regulatory submission support. Quantify study size, enrollment, audit outcomes, and compliance metrics without claiming CTM experience you do not have.
Skills to highlight
- ICH-GCP and FDA IVD/device regulations
- CRO and vendor management
- Site monitoring and oversight
- Clinical trial budgeting and forecasting
- TMF, CAPA, and audit readiness
- Protocol, ICF, and eCRF development
- Cross-functional collaboration
- Risk-based monitoring
Role summary
Remote US-based Clinical Trials Manager overseeing biomarker and IVD kit clinical studies from start-up through close-out, including CRO/vendor management, site oversight, budgets, GCP/FDA compliance, TMF maintenance, and regulatory submission support.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.