Senior Medical Director, Oncology Clinical Development (GI)

Role: Lead clinical development activities for AbbVie's therapeutic programs, overseeing trial design, execution, data interpretation, and regulatory compliance. Responsibilities: manage clinical study operations, ensure data integrity and safety monitoring, contribute to protocol and regulatory document development, and provide scientific expertise on disease areas. May oversee Medical and Scientific Directors, serve on Clinical Strategy Teams, and engage with external opinion leaders. Qualifications: MD or DO with at least 2 years of clinical trial experience in pharma, academia, or equivalent; strong knowledge of clinical trial methodology, regulatory standards, and GCP; excellent communication skills. High-Value: Focus on immunology, oncology, and neuroscience, with involvement in global clinical trials, regulatory interactions, and cross-functional team leadership. WorkSetup: Not specified.