# Clinical Trial Manager at Repertoire Immune Medicines

- Company: Repertoire Immune Medicines
- What the company does: Repertoire Immune Medicines is a clinical-stage biotechnology company working to unlock and direct the remarkable power of the human immune system to prevent or treat cancer, as well as autoimmune and infectious disease. Backed by SoftBank VF.
- Company website: https://www.repertoire.com/
- Type: Startups
- Level: Senior
- Location: Remote (US)
- Work setup: Remote
- Pay: $112K to $160K base salary per year (USD)
- Posted: 2026-09-06
- Apply by: 2026-10-21
- Apply: https://repertoireimmunemedicinesinc.applytojob.com/apply/UgERJpVyPm/Clinical-Trial-Manager
- Page: https://www.1752.vc/careers/jobs/repertoire-immune-medicines-clinical-trial-manager/

## About the role

We are seeking an experienced Clinical Trial Manager to provide both strategic leadership and hands-on oversight of early-stage oncology trials, including first-in-human trials. Reporting to the Director of Clinical Operations, you will oversee all aspects of trial management -from start-up through close-out - ensuring trials are delivered on time, on budget, and fully compliant with regulatory and quality standards.

## What they're looking for

- Work with a cross-functional trial teams to manage all aspects of clinical trials ensuring trials are executed on time, on budget, and in compliance with SOPs, ICH/GCP, and regulatory requirements
- Identify and anticipate trial issues or risks that may impact budget, resources, and timelines, plan mitigation strategies with the cross-functional team and escalates as necessary
- Manage trial budgets and contracts, including forecasting, invoice review, and expense tracking for accurate reporting
- Monitor trial progress, including participant enrollment, clinical data review, sample collection, and adherence to timelines, provide regular trial status updates and metrics
- Guide trial teams and investigator sites to ensure consistent interpretation and execution of trial protocols and procedures
- Contribute to the development and review of trial-related documents (protocols, ICFs, clinical trial plans, CRFs, manuals, reports, and regulatory documentation)