Freelance Clinical Research Associate (Germany)
Role summary by JobGrid
Freelance Clinical Research Associate (Germany) at Rho Inc: Remote, Germany; Contract; Mid; Healthcare & Science. JobGrid adds normalized role facts, source context, and a path to the employer application page so candidates can compare the listing before applying.
- Location and workplace: Remote, Germany
- Role classification: Healthcare & Science, Contract, Mid
- Source freshness: checked by JobGrid on 2026-06-10.
- Application path: candidates continue to the employer application page with non-personal referral tags.
Join us in redefining what it means to work for a CRO.
When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do.
Whether you’re a data wizard, analytical genius, healthcare advocate, project mastermind, or any other role, you’ll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other.
You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career.
We are currently hiring a Freelance Clinical Research Associate in Germany to join our amazing team! For this role, we will require circa. 0.85 FTE. Experience in Major Depressive Disorder would be preferred.
Our Clinical Operations will tell you that joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group!
What You Will Be Doing:
- Site administration and site monitoring responsibility for assigned clinical studies according to Dokumeds and Sponsor Standard Operating Procedures, legal requirements and ICH-GCP Guidelines
- Conduct of country and site feasibility
- Site initiation, routine monitoring and close-out visits
- Preparation and submissions to Ethics Committees/Regulatory Authorities
- Assistance in site contract management