Medical Director, Gastroenterology, non-MD - Pfizer : Job Details

Reporting to the US Specialty Care (US SC) Medical Lead for Gastroenterology, Biosimilars, and Rheumatology within headquarters, the Director, Rheumatology will be an integral member of the GI/Biosims/Rheum Medical Affairs team supporting current in-line assets (Xeljanz, Inflectra, and Abrilada), as well as pipeline assets depending on business needs and priorities.

The Director will develop long-term relationships with a wide variety of key healthcare stakeholders and customers, including professional organizations, patient societies, and key opinion leaders to demonstrate clinical and economic value of our assets. These activities are implemented to help inform HCPs and formulary decision-makers through medical presentations, pharmacoeconomic analyses, and outcomes evaluations along with the Organized Customer Group and Field Medical colleagues. Additional customer collaborations are built with the goal of aligning corporate medical priorities with the specific needs of the customer to advance the quality of patient care in areas of mutual interest, to identify provider and/or patient knowledge gaps, and areas for quality improvement interventions. The Director will develop, in conjunction with Medical team colleagues, an advanced perspective of the evolving clinical and healthcare landscape within Rheumatology and the Biosimilar space.

The Director will also provide Pfizer brand teams with customer and clinical insights to assist in informing Pfizer strategies on critical disease state related health issues and facilitate the development of customer-focused tools and medical communications to support patient access to quality medicines.

Role Responsibilities:

• Participate in reviewing & approving promotional and nonpromotional materials ensuring fair balance
• Collaborate with cross functional constituents from Commercial, Organized Customer, Field Medical to drive US strategic direction for the Brand
• Ability to plan and lead successful advisory boards, congress-related symposia & congress planning
• Ability to contribute to Publication planning, data generation activities and other medical/scientific activities related to informing HCPs on proper use of this potential new asset

Basic Qualifications:

• PhD, PharmD, DNP, or equivalent professional degree with 5+ years of experience in the pharmaceutical industry, clinical/medical practice, or combination of these
• Experience in clinical development or Phase IV/IIR trial management a plus
• Relationship builder within and outside of Pfizer
• Excellent presentation and communication skills
• Team oriented for success

Preferred Qualifications:

• Experience in Medical Affairs is preferred
• Experience in Gastroenterology is preferred
• Serve as a reliable, trusted source of accurate and scientific knowledge for the data, disease state, product label and competitive data sets for clinical trials
• Participate in developing and maintaining HCP engagement plans for HQ Medical Affairs

Other Job Details:

• Last Date to Apply for Job: August 27th, 2025.
• Ability to travel based on business needs (25%)
• NOT eligible for Relocation Package
• This position is hybrid and requires working onsite 2 to 3 days per week