What are the responsibilities and job description for the Director of Clinical Study Operations - 119425 position at Medix?
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 :
