Freelance Regional Clinical Trial Manager

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.

We are currently hiring a Freelance Regional Clinical Trial Manager to join our amazing team! In this role, you will oversee clinical trial operations and site management across multiple locations, ensuring compliance with regulatory guidelines, and working closely with Principal Investigators and clinical staff. You will be responsible for the successful execution of clinical trials, maintaining timelines and budgets while ensuring the highest standards of quality.

At Rho, our Regional Clinical Trial Managers are pivotal to our success, leading studies that can change lives and improve health outcomes for people around the world.

Responsibilities

• Oversee the planning, initiation, execution, and closure of clinical trials within your region
• Ensure compliance with GCP, FDA, and other applicable regulatory requirements
• Manage site selection, initiation, monitoring, and closing activities
• Collaborate with cross-functional teams to ensure efficient and effective trial operations
• Monitor trial progress and troubleshoot issues that may arise, providing timely solutions
• Develop and maintain strong working relationships with investigative sites and teams

Qualifications

• Degree in a related field (life sciences, nursing, etc.) with at least 5 years of experience in clinical trial management, preferably in a CRO or pharmaceutical environment.
• Proven experience managing regional or multi-site clinical trials successfully.
• Strong communicator with excellent written and verbal skills in English; knowledge of additional languages is an advantage.
• Detail-oriented with a commitment to quality and ethical conduct in clinical trials.
• High-Character: Collaborate with honesty and integrity; shown ability to build trust and work well within a team environment.
• Effective problem-solving and critical thinking skills, with the ability to adapt quickly to changing environments.
• Willingness to travel and have a valid driver’s license.

Please submit your CV in English. We’re excited to hear from you and to discuss how you can be a part of the Rho Factor!

Benefits

• A supportive and inclusive work environment with opportunities for personal and professional growth
• Competitive compensation based on experience
• Flexibility and autonomy in how you manage your work
• Engagement in impactful clinical trials that make a difference