2026 Physician Development Program - Endocrinology

AbbVie • North Chicago, IL

129d

About The Position

This role is based onsite at AbbVie's North Chicago, IL headquarters. AbbVie's Physician's Development Program (PDP) is a robust, two-year rotational program specifically targeting Medical Doctor (M.D.) specialist talent (graduating fellows). Those who have completed their M.D. program will also be considered. The goal of the program is to develop and support high-potential specialist physician talent in transitioning to a successful career within R&D at AbbVie. To that end, participants will engage in thoughtful, impactful rotational assignments within core R&D sub-functions, including Clinical Pharmacology & Pharmacometrics, Pharmacovigilance, Medical Affairs, Regulatory Affairs, and Clinical Development (both early and late stage). In addition to gaining critical cross-functional knowledge and exposure, the program also features a multi-level mentorship program and professional development sessions focused on honing leadership skills. This program and all rotations will be based at AbbVie's headquarters in North Chicago, IL. AbbVie is seeking physician talent with specializations in one or more of the following Therapeutic Areas: Oncology, Neuroscience, or Endocrinology. Participants will enter the program as Associate Medical Directors.

Requirements

• Medical Doctor (M.D.) or Doctor of Osteopathic Medicine (D.O.) degree.
• Completion of U.S. residency training by Spring 2026.
• U.S. board eligibility or certification (U.S. State or Commonwealth licensure).
• Strong verbal and written communication skills.
• Effective presentations skills.
• Ability to demonstrate critical thought processes and analytical skills.

Nice To Haves

• Medical specialty training in any of the following or related therapeutic areas: Oncology, Neurology, Immunology, Obesity, Endocrinology.
• Fellowship training associated with clinical research.
• Additional healthcare/research academic degrees, including PhD or MPH.
• A commitment to pursuing a career in clinical research.
• Experience publishing research.
• Demonstrated leadership skills.

Responsibilities

• Help design and implement study protocols for a development program in support of the overall Product Development Plan.
• Oversee project-related education of investigators, study site personnel, and AbbVie study staff.
• Help oversee clinical studies, supporting the monitoring of overall study integrity.
• Participate in design and execution of clinical trial safety, product safety, and risk management plans.
• Responsible for routine and ad hoc safety monitoring reports to regulatory agencies.
• Contribute to the design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents.
• Interact with and help coordinate appropriate scientific and medical activities with internal stakeholders.
• Assist in scientific/medical education of investigators, clinical monitors, and Asset Development Team members.
• Understand the regulatory requirements related to the clinical studies; accountable for complying with those requirements.
• Represent the medical function on cross-functional integrated teams for medical affairs activities.
• Assist in the development of scientifically accurate marketing materials, medical education programs, advisories, and symposia.

Benefits

• Paid time off (vacation, holidays, sick).
• Medical/dental/vision insurance.
• 401(k) to eligible employees.
• Short-term incentive programs.
• Long-term incentive programs.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Chemical Manufacturing
• Education Level: No Education Listed