My client (a growing publicly traded commercial biopharma company) is seeking a Medical Director, Medical Affairs . The individual will join a talented Medical Affairs team, reporting into the VP, Medical Affairs. This is a hands on, sole contributor role with no direct reports.

The role is remote with the ideal candidate living in the Northeast or Mid-Atlantic as you will need to travel to the NJ office 1 4 times a month (based on location).

Responsibilities:

Support post approval brand strategy and contribute to the planning, development, and execution of post approval studies

Support the evidence generation programs (i.e., Investigator Initiated Trials (IITs), post approval research, registries, and early access programs, etc.)

Participate in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy

Assist in the development, review, and approval of medical communications for scientific and clinical studies, HEOR, regulatory submissions, and post-approval market support

Partner with commercial as well as sales organizations to provide strategic medical insights to contribute shaping the portfolio strategy

Provide strategic input and medical due diligence to business development and licensing activities

Requirements:

MD

10 years of relevant experience within pharma or biopharma

Recent oncology experience (Lymphoma preferred)

Clearly communicate scientific results and effectively respond to data queries

Manage competing priorities and projects, including an ability to prioritize and manage expectations

Excellent verbal, written, and interpersonal communication skills

Experience in US and Global markets

Domestic and International travel up to 25% (conferences and corporate offices)

For more info, please reach out to chad.macdonald@adeccona.com

by Jobble