Sr. Clinical Trial Manager
Artiva Biotherapeutics · United States · US
Clinical Research
Remote
Nurse
Dentist
Demand78
Career growth72
Healthcare fit72
Remote potential45
Salary band
USD 165k – 185k
5-year outlook
Senior sponsor-side clinical trial management roles in biotech and cell therapy can offer strong compensation and progression toward Clinical Program Lead, Associate Director, or Director-level clinical operations. Exact salary varies by location, company stage, and experience.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-29
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, Dentist
- 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 considering for clinicians who already have substantial CRO, sponsor, or clinical trial management experience, especially in cell therapy, autoimmune, or rare disease. Clinicians without direct trial operations experience are unlikely to be competitive for this senior role.
Who should apply
Experienced clinical trial managers, clinical research nurses, physician-clinicians with sponsor/CRO trial operations experience, and advanced-degree healthcare professionals with 7+ years in clinical study management, vendor oversight, and global trial execution.
CV angle
Frame real clinical and research experience around sponsor/CRO oversight, ICH GCP and FDA compliance, site monitoring, protocol and CRF development, trial master file ownership, enrollment tracking, vendor management, cross-functional leadership, and any cell therapy, autoimmune, or rare disease exposure. Emphasize measurable trial deliverables and matrixed team leadership without overstating non-clinical experience.
Skills to highlight
- Clinical trial management
- ICH GCP and FDA regulatory compliance
- CRO and vendor oversight
- Site monitoring and site management
- Trial Master File and study documentation
- Protocol and CRF development
- Patient enrollment tracking
- Cross-functional and matrixed team leadership
Role summary
The Sr. Clinical Trial Manager leads operational execution of one or more clinical studies from protocol development through database lock, managing CROs and vendors, monitoring sites, ensuring GCP/FDA compliance, tracking enrollment, supporting data management, and coordinating study documents and investigator meetings.
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