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Medical Reviewer/Safety Reviewer III
3 months ago
Hours : 20-30 hours/week
Contract: 06 months contract
Purpose
In this role, you will support and manage projects, provide medical input on branded and unbranded content, and participate in various initiatives. You will represent medical affairs in the Medical, Legal, and Regulatory (MLR) review process to ensure compliance with industry regulations and guidelines
Qualifications:
1. Education: Advanced degree preferred (PharmD, PhD, PA, or NP).
2. Psychiatry, Epilepsy and Sleep/Wake Disorders research/experience is valued.
3. 3+years ad/promo medical review experience; Medical Review experience highly preferred (Veeva promo mat and med-com)
4. 3+ years of experience in the pharmaceutical industry or equivalent, with a strong understanding of medical affairs.
Responsibilities:
1. MLR Review: Represent medical affairs in the MLR process to ensure accuracy and compliance of commercial materials. Review promotional materials according to policies, guidelines, and customer needs.
2. Support Initiatives: Support projects such as MSL activities, medical education initiatives, digital communications, and conference preparations and reports.
3. Project Management: Lead assigned projects, ensuring timely and excellent results. Collaborate with cross-functional colleagues to align and execute projects.
