Associate Medical Director (Physician Development Program - Hematology)
Core
Two-year rotational program for M.D./D.O. specialists to transition into R&D roles at AbbVie, focusing on Clinical Pharmacology, Pharmacovigilance, Medical Affairs, Regulatory Affairs, and Clinical Development.
Role type
Associate Medical Director (Physician Development Program)
Builds
Clinical study protocols, safety plans, regulatory submissions, and medical education programs for oncology, neuroscience, and endocrinology therapeutic areas.
Domain
Biopharmaceutical R&D (Clinical Development & Regulatory)
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Medical Doctor (M.D.) or Doctor of Osteopathic Medicine (D.O.) degree, U.S. residency completion, U.S. board eligibility or certification, study protocol design, clinical study oversight, safety monitoring, regulatory compliance, scientific content analysis, cross-functional collaboration.
Preferred skills
Oncology/Hematology specialty training, clinical research fellowship, PhD or MPH, research publication history, leadership experience.
Technologies
Clinical trial management systems, regulatory submission platforms, statistical analysis tools.
Responsibilities
Design and implement study protocols, oversee project-related education of investigators and study staff, monitor study integrity and safety/efficacy data, participate in safety and risk management plans, prepare safety monitoring reports for regulatory agencies, contribute to clinical study reports and regulatory submissions, coordinate with internal stakeholders, represent AbbVie at external scientific meetings, assist in developing marketing materials and medical education programs.
Seniority
Entry-level rotational program participant (recent graduate/resident)