Medical Director/Scientific Director, Immunology Clinical Development

AbbVie is dedicated to discovering and delivering innovative medicines that address serious health issues. It operates across key therapeutic areas including immunology, oncology, and neuroscience. Job Description With supervision, oversees the direction, planning, execution and interpretation of clinical trials or research activities of a clinical development program. Participates in cross‑functional teams to generate, deliver, and interpret high‑quality clinical data supporting overall product scientific and business strategy. Responsibilities Manage the design and implementation of study protocols for a clinical development program based on medical and scientific principles, regulatory requirements, and emerging issues; oversee project‑related education of investigators, study site personnel, and AbbVie study staff. Oversee clinical studies, monitor overall study integrity, review, interpret, and communicate accumulating data related to safety and efficacy of the molecule; manage study enrollment and timelines for key deliverables. Contribute to design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions, and other program documents. Serve on a Clinical Strategy Team as the clinical representative for protocols subject to responsibility; collaborate in a cross‑functional, vetted clinical development plan. Participate in opinion leader interactions; partner with Medical Affairs, Commercial and other functions as required. Stay abreast of professional information and technology through conferences, literature, and training to augment expertise. Understand regulatory requirements related to the clinical studies and ensure compliance; contribute to regulatory responses and discussions. Ensure adherence to Good Clinical Practices, pharmacovigilance standards, SOPs, and all other quality standards in conducting research. Qualifications Medical Doctor (M.D.), Doctor of Osteopathy (D.O.), or non‑US equivalent; relevant therapeutic specialty in an academic or hospital environment; completion of a residency program strongly preferred, subspecialty fellowship desirable. Ability to run a clinical research study with appropriate supervision. Strong collaborative and cross‑functional communication skills. Experience in clinical trials within the pharmaceutical industry, academia, or equivalent. Knowledge of clinical trial methodology, regulatory and compliance requirements, and experience designing study protocols. Excellent oral and written English communication skills. Benefits Comprehensive benefits package including paid time off, medical/dental/vision insurance, and 401(k) for eligible employees. Participation in long‑term incentive programs. Equal Employment Opportunity AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. #J-18808-Ljbffr AbbVie