MSI are working with a large global pharmaceutical company to source for an experienced pharmacovigilance professional for a contract position as an Associate Director of PV processes. The core duties are to identify opportunities for and drive the enhancement of existing processes through knowledge of internal and external environment and lead the management of process updates in Patient Safety.

The ideal candidate would have:

• A science/pharmacy/nursing degree, with at least 5 years relevant experience (pharmaceutical, regulatory, safety and partnership)
• Experience in working cross-functionally
• Leadership skills, including proven leadership of project teams experience
• Thorough scientific knowledge sufficient to understand all aspects of regulatory/pharmacovigilance and partnership issues
• Thorough knowledge of the drug development process
• Good attention to detail
• Excellent written and verbal communication skills
• Proven ability to work across cultures
• Able to influence whilst maintaining independent and objective view
• Strong collaboration skills
• Strong negotiation, conflict management and interpersonal skills
• Relationship builder
• Able to work effectively as a member of a cross-functional or global team
• Understanding of change management process