Medical Writing Manager (Regulatory Writing)

IQVIA(6 months ago)

HybridFull TimeSenior$156,757 - $210,110 (estimated)Medical Writing

About this role

Lead Medical Writer at IQVIA responsible for overseeing and delivering high-quality regulatory and clinical documents in support of drug development. The role ensures documents meet IQVIA SOPs and customer requirements, provides senior review and mentorship to junior writers, and acts as a client-facing point of contact. The position also supports project-level budgeting, training, and cross-functional representation.

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Required Skills

Regulatory Writing
Clinical Writing
Document Review
Project Management
Stakeholder Communication
Budgeting
SOPs
Statistics
Detail Orientation
Negotiation

+1 more

Qualifications

Bachelor's Degree in Life Sciences
Master's Degree in Life Sciences (Preferred)
Ph.D. in Life Sciences (Preferred)

About IQVIA

iqvia.com

IQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.

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