# Study Manager at Evvy

- Company: Evvy
- What the company does: Get innovative vaginal healthcare, powered by our state-of-the-art Vaginal Microbiome Test. Our clinical care platform includes Rx for bacterial vaginosis (BV), yeast infections, aerobic vaginitis, fertility and more. Trusted by 100,000+ users. Backed by General Catalyst.
- Company website: https://www.evvy.com/
- Type: Startups
- Level: Senior
- Location: New York City
- Work setup: On-site
- Posted: 2026-05-18
- Apply by: 2026-10-08
- Apply: https://jobs.ashbyhq.com/evvy/54689871-9814-4bfd-8faf-f8a00175da53
- Page: https://www.1752.vc/careers/jobs/evvy-study-manager/

## About the role

We're looking for a Study Manager to run and manage Evvy's clinical study portfolio which includes both observational and interventional trials that generate the evidence behind our products. Reporting directly to the Co-founder & CSO, you'll be a critical hire on a small, high-leverage team, where the studies you run will directly shape what Evvy builds and launches.

## What they're looking for

- 5–7 years coordinating clinical studies, with hands-on experience across multiple study types (diagnostic validation, observational, and interventional preferred)
- Multi-site or CRO experience: you’ve run studies across multiple PIs and clinical sites and know how to optimize workflows
- A strong point of view on how AI can make clinical research faster and more rigorous, and a real track record of using it across protocols, site comms, and study reporting
- Women’s health, OB-GYN, fertility, or microbiome experience — ideally you understand the patients, the providers, and the clinical context
- IRB submission experience (WCG, Advarra, central, or local) and familiarity with EDC platforms
- Strong working knowledge of ICH-GCP, FDA, and HIPAA requirements, CCRC, CCRP, or ACRP certification preferred

Tags: Science / R&D