Job Description
📋 Description With supervision, directs clinical trials and research activities. Participates in cross-functional teams to deliver high-quality data. Manages study protocols for a clinical development program. Oversees safety and efficacy data review and timelines. Contributes to protocol design, reports and regulatory submissions. Stays current with regulatory requirements and GCP. 🎯 Requirements Bachelor's degree in sciences; MS/PhD preferred. Ability to provide input and direction with supervision. Strong collaboration in a cross-functional setting. Clinical trial experience in pharma or academia preferred. Knowledge of trial methodology and regulatory requirements. Excellent English communication, both oral and written. 🎁 Benefits Comprehensive benefits: PTO, medical/dental/vision, 401(k). Eligible for long-term incentive programs. AbbVie is an equal opportunity employer.
