Director of Clinical Study Operations - 119425

The ideal candidate will possess experience from the sponsor/CRO level with strong experience starting up study sites.

General Overview:

• Contribute to and exhibit best practices in study design and execution and manage the company’s live portfolio of projects
• Manage and collaborate with an evolving staff of clinical project managers, coordinators, and associates to achieve all study requirements and goals.
• Ensure strong compliance with regulations and protocols
• Collaborate with study consultants and sub-awardees and serve as an example for the rest of the team in how work is conducted.
• Oversee study budgets and timelines and recommend course corrections as necessary.
• Contribute to publication strategies and communications with outside stakeholders.

Experience:

• 10-15 years of experience in clinical research activities within leading life science companies including biopharmaceuticals, diagnostics/medical devices, and/or clinical research organizations.
• Successful roles leading multidisciplinary teams across geographies and serving as a department head, mentor, and coach to staff.