Medical Affairs Associate Director – Final Medical Approver
📍 Durham, North Carolina (Home-Based)
Job ID: R1497886
Job Type: Full-Time
Work Arrangement: Remote (occasional onsite client visits may be required)
Available in Additional Locations
As a Final Medical Approver within IQVIA’s Pharma Review Team, you will serve as the primary medical and scientific expert for US promotional and medical content, ensuring alignment with regulatory requirements (FDA/FDCA, PhRMA, FTC) for pharmaceuticals and medical devices. You’ll collaborate with cross-functional stakeholders and provide high-level approval and advisory services to pharmaceutical clients.
Serve as lead Medical Reviewer/Approver on content review committees.
Provide final medical/scientific approval of promotional assets in accordance with FDA, PhRMA, FTC guidelines and client strategy.
Offer second opinions and expert judgment on complex submissions.
Work closely with Commercial, Regulatory, and Legal teams to ensure aligned, compliant content.
Participate in client meetings as the medical representative.
Advise clients and teams on best practices in approval processes.
Support recruitment and onboarding of new reviewers.
Mentor and coach junior team members in both technical and leadership skills.
Represent medical affairs in internal training and audit initiatives.
Maintain up-to-date expertise on FDA/PhRMA/FTC promotional regulations and evolving healthcare industry practices.
Support internal and client audits in coordination with the Compliance team.
Champion core IQVIA compliance values.
Manage and track personal workload through timesheets and operational tools.
Escalate complex or high-risk issues to the Medical Director when necessary.
Use systems like Veeva Promomats and/or Aprimo for material review (experience preferred).
🎓 Advanced Science or Medical Degree Required:
PharmD, PhD, MD, NP, PA, RN strongly preferred
📆 Experience:
3–5 years of direct US promotional/medical review experience
Experience working independently with minimal supervision
📋 Regulatory Knowledge:
Advanced understanding of FDA, PhRMA, and FTC promotional guidelines
🔍 Research & Analysis:
Demonstrated ability to critically assess research design and clinical data
🖥️ Technology Proficiency:
Experience with Veeva Promomats and/or Aprimo is desirable
💵 Annual Salary Range:
$112,000 – $312,000 USD
(Final offer based on experience, education, location, and other job-related factors)
Additional compensation may include:
Incentive plans
Bonuses
Comprehensive health and welfare benefits
IQVIA is a global leader in clinical research, real-world evidence, and healthcare data analytics. We partner with life sciences companies to deliver innovative medical solutions and accelerate their path to market.
IQVIA is an Equal Opportunity Employer. We welcome applicants of all backgrounds and do not discriminate based on race, religion, sex, gender identity, sexual orientation, national origin, veteran status, or disability.
🔗 Click here to apply
Job ID: R1497886
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