Research Manager, Startup Regulatory Operations
UNAVAILABLE · United States · US
Clinical Research
Remote
Dentist
Demand82
Career growth76
Healthcare fit80
Remote potential95
Salary band
USD 99k – 157k
5-year outlook
Manager-level clinical research regulatory roles in academic cancer centers generally offer stable compensation and moderate advancement into research operations leadership; exact pay varies by location, experience, and institution.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-21
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 with clinical research, IRB, or regulatory startup experience who want a remote non-clinical operations role; clinicians without trial/regulatory exposure may find the manager-level expectations steep.
Who should apply
Research nurses, clinical research coordinators, physicians or pharmacists with trial/regulatory experience, and IMGs/healthcare graduates who have supported IRB submissions, study startup, or GCP-compliant documentation.
CV angle
Frame real clinical research involvement as regulatory operations experience: IRB submissions, protocol/consent review, essential document management, GCP training, audit/inspection preparation, and cross-functional coordination with investigators, sponsors, and ancillary teams. Avoid claiming startup management you have not done.
Skills to highlight
- Clinical research operations
- Regulatory startup and study activation
- IRB submissions and protocol review
- Good Clinical Practice (GCP) compliance
- Essential document and investigator file management
- Audit/inspection readiness
- Cross-functional project coordination
- Regulatory timeline and risk management
Role summary
Manages regulatory startup and activation for clinical research studies, coordinating IRB submissions, essential documents, training, and cross-functional approvals to ensure compliant and timely study activation.
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