Clinical Trials Manager, Clinical Operations
Bristol Myers Squibb · United States · US
Clinical Research
Remote
Dentist
Demand80
Career growth78
Healthcare fit82
Remote potential35
Salary band
USD 135k – 163k
5-year outlook
Likely competitive within biopharma clinical operations, with progression toward Clinical Operations Program Lead/Head; compensation depends on location, oncology/radiopharma experience, and CRO/vendor management track record.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
full-time
Date found
2026-10-18
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- United States
- Profession fit
- 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 applying if you already have 5+ years in clinical research/operations or CRO/site management and want biopharma trial leadership; not a realistic entry point for clinicians without industry trial experience.
Who should apply
Oncology nurses, physicians, pharmacists, or allied health professionals with 5+ years in clinical research, site coordination, CRO/vendor management, or trial operations; IMGs with equivalent clinical operations experience may also fit.
CV angle
Frame real experience around trial lifecycle ownership, site feasibility/activation, enrollment and data quality oversight, GCP/ICH/FDA compliance, CRO/vendor management, budget/invoicing, risk mitigation, and cross-functional leadership; quantify study size, phases, and timelines where possible.
Skills to highlight
- Clinical trial management
- CRO and vendor oversight
- GCP/ICH/FDA compliance
- Site feasibility and activation
- Study timelines and budgets
- Risk mitigation and issue escalation
- Cross-functional team leadership
- Oncology/radiopharmaceutical clinical operations
Role summary
Manages Phase I-III clinical trials for an oncology radiopharmaceutical biotech, including CRO/vendor oversight, site feasibility and activation, timelines, budgets, enrollment, data quality, risk mitigation, and GCP/FDA compliance.
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