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.
Must-Have Qualifications & Skills: 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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