AI agents that run your enterprise workflows and get measurably better over time. 150+ enterprises live in production across retail, insurance, and financial services. Backed by Accel and General Catalyst.
About the role
You’ll take full ownership of your assigned trial(s) — from protocol development to close-out — with the autonomy to make daily calls and the support of an experienced team when it counts. The posted range applies to roles based in the San Francisco Bay Area and reflects local market conditions. Where an offer lands within that range depends on the candidate’s relevant experience, technical expertise, and how their background aligns with the role’s requirements. Found on 1752vc Careers, the job board for startup and VC roles.
What they're looking for
- Own all operational aspects of your assigned clinical trial(s)
- Manage day-to-day CRO/vendor relationships to keep deliverables on budget, timeline, and protocol
- Build strong working relationships with site investigators and study coordinators
- Track trial progress and keep stakeholders updated on status
- Monitor enrollment and address recruitment challenges as they arise
- Manage study budget, forecasting, accruals, and vendor payments for your trial(s)
More about this role
Clinical Trial Manager (CTM)
You’ll take full ownership of your assigned trial(s) — from protocol development to close-out — with the autonomy to make daily calls and the support of an experienced team when it counts.
This individual is responsible for the management of assigned clinical trial(s), leading the study team, vendors, clinical monitors, and clinical sites throughout the trial lifecycle.
- Own all operational aspects of your assigned clinical trial(s)
- Manage day-to-day CRO/vendor relationships to keep deliverables on budget, timeline, and protocol
- Build strong working relationships with site investigators and study coordinators
- Track trial progress and keep stakeholders updated on status
- Monitor enrollment and address recruitment challenges as they arise
- Manage study budget, forecasting, accruals, and vendor payments for your trial(s)
- Partner with Data Management on CRF content, completion guidelines, and data deliverables
- Draft and coordinate review of protocols, informed consents, CRFs, monitoring plans, and study reports
- Prepare for and support regulatory agency audits and inspections
- Flag risks early and recommend solutions before they become...
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