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Posted 3 hours agoNational Manager, Sites - India
Mumbai, IndiaOn-site
Responsibilities
- Launch the Iterative Health site support organization structure in India .
- Support hiring and onboarding of Clinical Research Coordinators (CRC) for each site in the network. Supervise and mentor CRCs across studies and site network
- Oversee and manage all aspects of study execution from startup to close-out across the site network to ensure timely delivery, highest quality and adherence to protocols.
- Conduct routine oversight visits (on-site/remote) across network sites to review study progress, CRC performance, review protocol compliance, ensure audit readiness, escalate issues promptly, and maintain the highest quality of deliverables throughout the clinical trial lifecycle.
- Drive subject recruitment and retention strategies, ensuring monthly enrollment goals are met across clinical sites.
- Drive PI engagement on Iterative Health trials by providing proactive, hands-on support to principal investigators — helping them navigate study requirements, resolve questions, and stay closely connected to trial progress.
- Support pre-feasibility assessment and provide actionable operational insights including availability of patient pool, investigator competence and therapy experience, site capability and infrastructure to select best sites for new studies.
- Perform other tasks as assigned
Requirements
- By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.
- By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.
- Experience: Minimum 8 years of project management, site management experience in clinical research.
- experience in site management and leading teams of site coordinators and operations staff.
- Strong technical knowledge, robust understanding of clinical trial processes, GCP, and country and international regulatory requirements.
- Ability to manage multiple studies/sites •
- Experience of managing clinical trials in Gastroenterology, Cardiology will be a strong plus.