Job Description
📋 Description Initiates medical affairs activities, data generation and dissemination of data for scientific Design, analysis, interpretation, and reporting of protocols, Investigator Brochures, Clinical Oversees Medical Affairs-led clinical studies; monitors study integrity and safety/efficacy data Provide in-house clinical expertise; coordinate with internal stakeholders; collaborate on Interact with leaders to incorporate cross-functional perspectives into Clinical Development Plans. Assist in developing scientifically accurate marketing materials and medical education programs. 🎯 Requirements Advanced Degree PhD or PharmD; post-doctoral experience preferred. 7-10 years in Medical Affairs with Global Medical Affairs experience preferred. Typically 10-15 years in pharma; strong understanding of therapeutic area. Minimum 4 years of clinical trials direct management; 4+ years preferred. Knowledge of clinical trial methodology, data analysis and regulatory requirements; protocol design Ability to run a clinical study independently; proven cross-functional leadership. 🎁 Benefits AbbVie offers a comprehensive benefits package including paid time off, medical/dental/vision Eligible to participate in long-term incentive programs. Equal Opportunity Employer; information on accommodations available on company site.
