Some key responsibilities of the role will include:

• Serve as a clinical lead, responsible for the oversight of all operational aspects of clinical trials.
• Manage CRO/vendor interactions, including sponsor oversight of delegated responsibilities, scope revisions/contract amendments, budgets and invoices, etc.
• Monitor study progress, review emerging clinical data, and ensure data retrieval and clean-up is completely on schedule.
• Ensure that assigned clinical trials are executed in compliance with applicable regulations, guidance and SOPs. Travel to vendor and investigative sites to conduct on-site QC visits at clinical trial vendor facilities and investigative centers.

The ideal candidate should have a Bachelor's degree in a scientific discipline or related field with 5+ years clinical research experience, including two years in a managerial role.