Senior Director/Director, Patient Reported Outcomes (PRO): Pfizer

June 1, 2010

Location: Groton, Connecticut; New York, New York, USA
Reference number:: 939229
Full/Part Time: Full-Time

Responsibilities

The Senior Director would oversee a therapeutic area and may have staff reporting to them
Senior Director/Director:
Will manage PRO projects for multiple products within a therapeutic area, in conjunction with HEOR staff
Generate study proposals and designs for multiple products.
Analyze, communicate, and publish impactful research pertaining to assigned products.
Contribute to the market access strategy development
Align PRO activities with the market access strategy
Display technical competency in at least two of the following: systematic reviews, qualitative research, psychometrics, or statistics.
Establish a technical mastery in one of the following disciplines: qualitative research, psychometrics, or statistics.
Strong technical competency in use of ePROs and cross-cultural validation of PROs
Contribute to valuation assessments of BD opportunities and disease area profiles in terms of PRO challenges
Point contact for SEALD interactions within a therapeutic area
Manage project budget and timelines

Qualifications

Senior Director:

Masters degree in Psychology, or related discipline; doctoral degree strongly preferred
8 years pharma experience or closely related experience, across multiple products and/or therapeutic areas
Clinical development experience of implementing PRO strategy essential
People management preferred
Regulatory experience in negotiating PRO label claims/promotional claims essential Director:
Masters degree in Psychology, or related discipline; doctoral-level degree preferred
5 years pharma experience or closely related experience, across multiple products and or therapeutic areas
Clinical development experience of implementing PRO strategy
Regulatory experience in negotiating PRO label claims

Please forward resumes to carol.beck@pfizer.com