Job Description
📋 Description Leads direction, planning, execution, and interpretation of clinical trials or research activities Leads cross-functional teams to generate and disseminate high-quality clinical data supporting Owns design/implementation of multiple clinical development programs and study timelines. Oversees study teams, data safety/efficacy review, and regulatory communications. Responsible for scientific content of protocols, CSRs, and regulatory submissions. May supervise Medical/Scientific Directors and Clinical Scientists. 🎯 Requirements MD/DO or non-US equivalent with oncology focus; residency preferred; oncology fellowship desirable. 5+ years (7 preferred) of clinical trial experience in pharma/academic settings. Ability to lead a complex clinical research program independently. Strong leadership and cross-functional collaboration skills. Experience with clinical trial methodology, regulatory/compliance knowledge, and study protocol Excellent written and verbal English communication. 🎁 Benefits Comprehensive benefits package including PTO, medical/dental/vision insurance, and 401(k). Eligibility for long-term incentive programs. AbbVie is an equal opportunity employer; inclusive workplace policies apply.
