PV Partnerships Associate 

• Excellent junior opportunity 
• Office based in Maidenhead
• Career progression in PV, Regulatory Affairs or Medical Affairs 

Role Overview

Act as the responsible contact for Business Units (Medical Affairs, Market Access, Patient Engagement, Legal department) in initiating, organizing and managing Organized Data Collection (ODC) projects.

Support the UK Pharmacovigilance Team on the coordination and execution of all aspects of the PV system to ensure that all of AbbVie’s statutory and ethical responsibilities are met.

Key Responsibilities  

• Key point of contact for AbbVie across patient support vendors
• Responsible for review of commercial projects for PV requirements
• Market Research colleagues; all areas of organized data collection
• Support of team in PV adverse events (UK) note taking and entering information into database, code and exhibited
• Collaborates with the PV Compliance and Training Manager and/or Specialist to ensure Pharmacovigilance training is provided
• Monitors and ensures the compliance of Service Providers concerning Pharmacovigilance tasks (AE reporting compliance, reconciliation, program close out etc.)

• Degree in life sciences, or relevant industry experience.  Preferred background, but not essential, Nursing or Pharmacist
• Pharmacovigilance experience desirable, or experience in a Patient Support Program company
• Team-oriented
• Ability to prioritize, strong planning and excellent organizational skills and the ability to get things done
• Ability to develop and maintain strong collaborative relationships with internal and external stakeholders
• Good communicator and stakeholder management