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! In this role, you will have the opportunity to manage all aspects of study site management including site selection, initiation, routine monitoring, close-out and maintenance of study files. You’ll also ensure the quality and integrity of data, compliance with relevant SOPs and regulatory requirements and study completion on time and within budget.
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:
Please submit your CV in English. We’re excited to hear from you!
We offer:
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Join us at Rho as a Freelance Clinical Research Associate in Germany, where we’re redefining what it means to be part of a Contract Research Organization (CRO). Here, every day is an adventure filled with curiosity and innovative thinking. As a member of our dynamic team, you’ll be immersed in a culture that believes in teamwork and collaboration, blending science with a sprinkle of fun. In this role, you will manage the entire study site lifecycle, from selecting and initiating sites to monitoring and closing them out—ensuring that data quality and compliance never take a back seat. You’ll be supported by our incredible Clinical Operations team, and together, you’ll strive for excellence in meeting regulatory requirements. Imagine being a part of a community that values your insights and well-being, where financial stability is just as important as creativity and professional growth. If you’re a passionate individual with a background in medicine, pharmacy, nursing, or life sciences, and at least two years of monitoring experience, we want to hear from you! Your ability to communicate effectively in both English and local languages, along with a keen eye for detail, will make you a valuable asset to the Rho Factor. Embrace the opportunity to thrive in an agile environment where you can drive your career forward, laugh with your colleagues, and realize the true potential of your professional journey. We can’t wait to have you on board!
We are looking for a Regulatory Consultant to join our dynamic team at Rho, dedicated to transforming the landscape of healthcare and clinical research.
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To improve health, extend life, and enhance the quality of life via corporate and research excellence.
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