Patient Reported Outcomes Management Associate

2 weeks ago


Madison Wisconsin, United States AbbVie Full time
Job Summary

The Patient Reported Outcomes Management Associate III is a key member of the Clinical Program Development (CPD) team at AbbVie, responsible for driving and managing deliverables related to patient reported outcomes (PRO) and electronic patient reported outcomes (ePRO) processes. This role requires expertise in PRO/ePRO licensing, translation, and implementation to ensure timely and cost-effective study start-ups.

Key Responsibilities
  • Provide consultation and support for PRO licensing and translation activities across various therapeutic areas within CPD.
  • Manage the Vault PRO Library, a repository of PROs, including licensing and permission details, MSAs with AbbVie, translation requirements, training requirements, and electronic format requirements.
  • Collaborate with PRO owners, Outsourcing, HEOR, Data Sciences, and clinical teams to drive PRO and ePRO implementation, including vendor contract initiation, translation management, project milestones, timelines, and deliverables.
  • Offer strategic and technical expertise and training to the CPD organization in support of PRO/ePRO activities during study start-up.
Requirements

This role requires a strong understanding of PRO/ePRO processes, excellent communication and project management skills, and the ability to work effectively in a team environment. The ideal candidate will have experience in clinical data management, PRO licensing, and translation management.


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