Associate, Study Management II
AbbVie · United States · US
Clinical Research
Remote
Dentist
Demand84
Career growth82
Healthcare fit87
Remote potential88
Salary band
USD 85k – 162k
5-year outlook
Likely stable to strong within pharma and CRO clinical operations, with advancement toward Study/Project Manager or Clinical Trial Lead roles improving long-term earning potential; exact pay depends on country, experience, and sponsor/CRO.
Clinical license
Not required
Applicant reach
moderate
Seniority
junior
Employment type
full-time
Date found
2026-10-28
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
Yes for clinicians interested in sponsor-side clinical trial operations and a path toward study/project management. Prior research, GCP, site coordination, or CTMS/eTMF exposure would make the application stronger.
Who should apply
Clinicians with clinical trial exposure, research coordinators, nurses or pharmacists interested in pharma clinical operations, IMGs/healthcare graduates with GCP or site-level research experience, and allied health professionals seeking non-patient-care clinical research roles.
CV angle
Emphasize protocol-driven care, ICH/GCP exposure, patient recruitment and retention, documentation accuracy, adverse event/reporting workflows, multidisciplinary coordination, data quality, regulatory compliance, and any site/study coordination or stakeholder management experience. Translate clinical workflows into clinical trial execution, risk management, and inspection-readiness language without claiming unheld study management experience.
Skills to highlight
- Clinical trial operations
- ICH/GCP compliance
- Cross-functional study coordination
- Vendor and stakeholder management
- CTMS/eTMF documentation
- EDC/IRT/ePRO systems
- Patient recruitment and retention
- Risk management and inspection readiness
Role summary
A pharma sponsor-side clinical research operations role supporting global Phase 0-4 trials from planning through closure, including vendor oversight, recruitment strategy, study documentation, CTMS/eTMF systems, risk management, and cross-functional meeting coordination.
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