Global Head Medical Affairs

Responsibilities

• Lead, manage and develop a best-inclass, high-performance medical writing, medical affairs team and related support functions;
• Provide strategic direction to the Executive Leadership Team and Board of Directors on all Medical Affairs matters;
• Provide medical support for key clinical activities; including broad scientific/medical support for clinical studies including HNV, Phase I-IV programs;
• Build, direct, and oversee the activities of Therapeutic science liaison functions.
• Oversee clinical trials by designing the programs, monitoring them for safety, reporting adverse events and providing documentation to regulatory agencies;

Requirements

• Minimum of 5-7 years in a CRO or pharmaceutical/biotech sales or operations;
• Experience and knowledgeable in managing the medical affairs requirements of both early phase clinical and late phase clinical business development;
• Advanced understanding of clinical medicine/clinical pharmacology, and associated disciplines (e.g., biostatistics) drug development principles.