Key Responsibilities:
- Ensure accurate, timely, and compliant responses to complex medical inquiries across EMEA for assigned therapeutic areas.
- Manage medical information content in line with global strategies, product lifecycle stages, and regulatory milestones.
- Oversee medical information providers and ensure alignment with KPIs, performance standards, and quality expectations.
- Support the implementation of innovative digital technologies, channels, and systems aligned with GMI’s digital strategy.
- Train and support affiliates and vendors on EMEA-specific processes and best practices in medical information delivery.
- Advanced scientific or medical degree (e.g., PharmD, PhD, MD, or equivalent).
- Minimum 5 years of relevant experience, with at least 4 years in the biopharmaceutical industry and 2 years in medical affairs, clinical research, or pharmacovigilance.
- Proven experience in managing vendors and leading complex cross-functional projects.
- Strong understanding of medical information best practices, applicable legal and regulatory requirements, and industry codes of practice.
- Exceptional communication skills, including scientific writing and stakeholder engagement in a matrix organization.
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