Clinical Trials Associate (or Senior)
BioAge Labs · United States · US
Clinical Research
Remote
Dentist
Demand72
Career growth74
Healthcare fit82
Remote potential35
Salary band
USD 80k – 90k
5-year outlook
Clinical operations experience can progress toward Clinical Trial Manager or Clinical Program Manager roles, with compensation rising alongside trial complexity, CRO oversight, and inspection-readiness responsibility; exact figures depend on location, company stage, and level.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-11-08
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- Dentist
- Rate period
- Annual
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 for clinicians who already have site-level research, CRO, or biotech clinical operations exposure and want a clear non-clinical path into clinical trial delivery. Less suitable for clinicians with no TMF, CTMS, EDC, or GCP-based trial operations experience.
Who should apply
Research nurses, clinical research coordinators, pharmacists with trial experience, physicians with site or sponsor trial exposure, IMGs with GCP/clinical research familiarity, and healthcare graduates with 2–3 years in CRO, biotech, pharma, or site clinical operations.
CV angle
Reframe real clinical work into clinical operations language: site coordination, protocol adherence, ICH/GCP compliance, IRB/IEC documentation, source-to-TMF quality, EDC data accuracy, lab sample handling, vendor/CRO communication, audit preparation, and cross-functional timeline tracking. Do not claim sponsor-level or CRO oversight experience unless genuinely held.
Skills to highlight
- TMF/eTMF quality control
- CTMS and EDC familiarity
- ICH/GCP compliance
- IRB/IEC submissions and regulatory documentation
- CRO/vendor and site coordination
- Clinical trial start-up through close-out support
- Inspection and audit readiness
- Laboratory sample tracking and reconciliation
Role summary
A sponsor-side clinical operations role supporting Phase 1–3 trials by coordinating sites, CROs, vendors, regulatory documents, TMF quality, study systems, timelines, and inspection readiness.
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