Medical Director / Scientific Director, Medical Affairs - Precision Medicine

AbbVie•Mettawa, IL

1d•$160,500 - $305,000•Hybrid

About The Position

AbbVie is seeking a dynamic Medical Director / Scientific Director for Medical Affairs, Precision Medicine, to lead U.S. CDx strategy in oncology. This role requires a strong background in diagnostics, pathology, biomarkers, and cancer therapeutics, as well as a demonstrated commitment to precision medicine. This position must be based at our Mettawa, IL headquarters and will follow a hybrid schedule of 3 days/week in office.

Requirements

Scientific Director: Bachelor’s Degree in the sciences. Advanced Degree PhD, PharmD, PA or NP preferred. Residency or additional post doctorate experience preferred. 5-7+ years of experience in the diagnostic or pharmaceutical industry, or equivalent; substantial understanding of oncology or precision medicine required.
Medical Director: Medical Doctorate (M.D.) degree or equivalent (D.O. or non-US equivalent of M.D.) required. Relevant therapeutic specialty in an academic or hospital environment preferred. Completion of residency and/or fellowship preferred. 0-2+ years of experience in the diagnostic or pharmaceutical industry, or equivalent.
Strong leadership abilities, including influence without authority in cross-functional teams, prioritization, coaching, mentoring, and conflict resolution.
Clear demonstration of cross-functional and team-focused partnership and collaboration
Experience with companion or complementary diagnostics, ideally in the oncology space.
Experience working with testing landscape stakeholders, including diagnostic partners, academic and community pathologists, precision medicine oncologists, and reference labs.
Demonstrated publication record and/or leading evidence generation projects
Excellent verbal and written communication skills, with emphasis on medical communication.

Nice To Haves

Prior experience in Medical Affairs within a diagnostic company, reference laboratory, or other functions in pharma is desirable.

Responsibilities

Lead and deliver a comprehensive, U.S. focused medical strategy for CDx-dependent indications overseeing execution of key deliverables.
Develop and implement the Medical Affairs strategy for upcoming CDx launches.
Build and maintain key external relationships with diagnostic partners, academic and community labs, and reference labs.
Cultivate relationships with expert pathologists and key opinion leaders.
Forge strong partnerships with leading pathology societies
Represent Medical Affairs in cross-functional Oncology Precision Medicine teams across the organization.
Act as the medical affairs lead on the Integrated Brand team and Medical Affairs team.
Develop and execute a biomarker and CDx evidence generation plan in collaboration with Precision Medicine Development, Health Economics and Outcomes Research, and Therapeutic Area teams.
Execute key functional deliverables aligned with the CDx medical strategy, including: Evidence generation to address biomarker and testing gaps, Medical review of scientific publications, Educational initiatives for both internal and external audiences on biomarkers and testing, Review of medical promotional materials for biomarker and testing content, Collaboration with Value and Evidence teams on guideline strategies for biomarkers and testing, Insight generation via advisory boards and engagements with external experts.
Develop and implement a congress strategy for pathologists, including EE engagements and digital initiatives.
Support oncology congresses with biomarker and testing materials in partnership with the Therapeutic Area team.