Sr. Study Management Specialist

📋 Description

• Manage and Lead complex and high-priority studies on all aspects of design, planning, startup
• Provide comprehensive input to study concept development especially from an operational
• Develop and manage study documentation throughout the study lifecycle, including protocols
• Serve as the operational point of contact for MFDS for regulatory PMOS.
• Lead the end-to-end operational management of assigned studies from concept through final reporting.
• Lead study start-up activities and oversee vendor, CRO and study-site selection, set-up and

🎯 Requirements

• University degree or equivalent; preferably in a medical/science-related field
• Minimum 7-year experience in clinical research in healthcare, pharmaceutical and/or CRO industry or
• Demonstrated experience independently managing complex studies is preferred
• NIS experience is preferred
• Fluent English communication skills (Reading, writing, speaking)
• Good understanding of clinical trial processes, AbbVie internal processes and the regulatory

🎁 Benefits

• Equal Opportunity Employer/Veterans/Disabled