# Senior Clinical Trial Manager, Cambridge, MA at Isomorphic Labs

- Company: Isomorphic Labs
- What the company does: Isomorphic Labs is building a future where frontier AI can help to unlock deeper scientific insights, faster breakthroughs, and life-changing medicines. Backed by GV.
- Company website: https://www.isomorphiclabs.com
- Type: Startups
- Level: Senior
- Location: Cambridge, MA
- Work setup: On-site
- Posted: 2026-08-26
- Apply by: 2026-10-10
- Apply: https://job-boards.greenhouse.io/isomorphiclabs/jobs/6163435004
- Page: https://www.1752.vc/careers/jobs/isomorphic-labs-senior-clinical-trial-manager-cambridge-ma/

## About the role

The Senior Clinical Trial Manager will fully understand and independently lead the cross-functional team through all activities within the clinical trial life cycle. These will include daily activities managing all trial start-up, conduct and close out activities to both industry and corporate standards within ICH/GCP Guidelines. The Senior Clinical Trial Manager may also have program responsibilities and managerial responsibilities, working in tandem with the Head of Clinical Operations as the department grows.

## What they're looking for

- Have the skillset and experience to execute/ manage execution of all related study start-up, maintenance and close out activities
- Demonstrates an AI-curious mindset, with an interest in exploring and leveraging emerging AI technologies to streamline contract lifecycle management and enhance operational efficiency
- Strategic and analytical thinker with excellent problem-solving capabilities and adaptability in fast-paced, matrixed environments
- Proven ability to build strong cross-functional relationships, mentor team members, and drive efficient business solutions across functional and regional boundaries
- Manage Change Orders and re-scoping with vendors and sites when necessary, including checking for accuracy of invoices and cost of services versus accruals
- Drive, contribute to and support the writing of all related clinical documents (such as the Protocol, ICF, DSUR, IB, CSR) for timely and accurate submission readiness

Tags: Clinical