Epidemiology Study Operations Manager
AbbVie · United States · US
Clinical Research
Remote
Dentist
Demand78
Career growth75
Healthcare fit72
Remote potential55
Salary band
USD 110k – 209k
5-year outlook
Pharma study operations and real-world evidence roles typically offer competitive, stable compensation with room to move into senior study leadership or epidemiology program management. Exact figures depend on location, pay-disclosure state, and internal banding, so candidates should confirm the full range with the recruiter.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-07
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 considering for clinicians with research, pharmacovigilance, or trial-coordination exposure who want to move into pharma study operations. The 6+ year experience and 2-year project management bars make it a stretch for early-career clinicians without operational or industry background.
Who should apply
Physicians, pharmacists, and nurses with prior clinical research, pharmacovigilance, or CRO/industry experience; IMGs and healthcare graduates who have coordinated studies, managed vendors, or supported regulatory documentation and want a pharma operations career path.
CV angle
Reframe real clinical and research experience around study coordination, protocol review, regulatory/IRB documentation, vendor or site communication, and timeline/budget tracking. Quantify any trial, audit, or quality-improvement work and emphasize cross-functional collaboration with safety, regulatory, and data teams, without overstating industry experience you do not have.
Skills to highlight
- Clinical study coordination and protocol review
- Project management and timeline tracking
- Vendor/CRO oversight and scope development
- Regulatory and IRB/EC documentation
- Budget and resource oversight
- Pharmacovigilance and risk management awareness
- Cross-functional stakeholder communication
- Clinical trial management systems and databases
Role summary
An operations-focused pharma role supporting Global Epidemiology's non-interventional, real-world evidence studies. The manager coordinates study deliverables, timelines, vendors/CROs, budgets, and regulatory documentation while partnering with safety and cross-functional teams to ensure compliance and quality.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.