Note: The job is a remote job and is open to candidates in USA. Priovant Therapeutics is committed to developing therapies for autoimmune diseases with high unmet need. The Associate, Clinical Operations will support late-stage clinical trials by driving operational and monitoring execution, maintaining study documentation and metrics, coordinating site and vendor activities, and supporting clinical operations workstreams.
Responsibilities
- Develop and maintain a system for organizing and tracking essential documents related to study start-up and execution
- Function as the first-round reviewer of IP release checklists, ensuring that all essential study documents meet compliance standards prior to site activation
- Support the timely execution of Priovant’s clinical development goals by managing and maintaining key study metrics around monitoring and data quality
- Help manage site-level interfacing with external vendors, such as troubleshooting site issues
- Support the clinical monitoring team by co-monitoring on key programs
- Facilitate tracking of operational on-study workflows, such as protocol amendment implementation and patient re-consenting
- Ad hoc support for clinical operations workstreams across programs
Skills
- Bachelor's degree (preferably in a scientific or technical discipline)
- Strong organizational skill set. Ability to manage multiple tasks and competing priorities
- Collaborative, with the ability to work well in small teams
- Extremely detail-oriented
- Flexibility to travel when needed (may support up to 2 on-site visits each month)
- Ability to learn quickly and respond well to feedback
- Proficiency with Excel, PowerPoint and project management software such as Monday.com
- Minimum of 2 years of clinical research experience – ideally 3-4 years
Company Overview
Company H1B Sponsorship