Associate Director responsible for ensuring scientific accuracy and compliance in global content approval. Collaborating with various teams to meet content quality standards in the biopharma industry.
Responsibilities
Ensure global promotional and non-promotional content meets the highest standards of quality, scientific accuracy, balance, and compliance
Act as primary medical reviewer and/or approver for Global promotional and non-promotional materials
Maintain deep scientific and therapeutic expertise on assigned products and therapy areas
Collaborate with business partners to align and validate content
Provide timely feedback and recommendations for content created and/or reviewed by third-party vendors
Stay up to date with evolving regulatory requirements, industry standards, and best practices
Requirements
Master’s/Graduate Degree in Life Sciences or Healthcare
4+ years of pharmaceutical industry experience
3+ years of Medical Affairs experience as a reviewer of content used in promotional and non-promotional settings
Understanding of the typical commercial and medical activities from a global perspective in the pharmaceutical industry (e.g., promotion, medical education, external partnerships, advisory boards)
Strong clinical literature evaluation skills
Benefits
Comprehensive benefits program GSK offers US employees
Job title
Associate Director, Content Approval, Specialty/Gen Med
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