Join us in redefining what it means to work for a CRO. Dokumeds has become part of Rho, an award-winning, full-service CRO based in North America. As one company, we will deliver global full-service clinical development services and unmatched customer support – worldwide. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges.

At Rho, we’re committed to you just as you’re committed to us. 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. With a collaborative team of smart, talented, and positive people, you’ll be celebrated and respected for your expertise and given the freedom to think creatively, challenge the norm, and problem-solve.

We are currently hiring a Freelance Regional Clinical Trial Manager to join our team in the EU. This is a remote position working on a freelance basis and we are seeking 1.0 FTE to start immediately.

Our Clinical Operations will tell you, 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!

• Manage international Phase I-IV clinical trials
• Plan and control clinical study budget
• Create and update project plans and timelines to ensure fulfilment of all commitments
• Manage the work within the Project Team and ensure all internal and external members performs their task during the study process according to agreed timelines and project requirements
• Monitor and oversee timely conclusion of site contracts and correct processing of payments
• Provide regular status reports to all relevant functions
• Prepare project management reports for clients and internal personnel/management
• Act as main point of contact for the Sponsor

• University degree in medicine, pharmacy, nursing or biology, along with at least 5 years of clinical trial experience in pharmaceutical, device, biotech or CRO setting, which includes at least 2 years’ experience in Project Management
• Strong leadership (including conflict management), organizational, interpersonal and communication skills, with an ability to prioritize and manage work for a team
• Strong Communicator: Demonstrate written, verbal and presentation skills to help showcase the successes of your work and Rho’s. Fluency in both English and local languages.
• Committed to Quality: Every job at Rho requires an attention to detail, a deep understanding of our high-quality scientific standards, and an ability to care about every outcome.
• High-Character: Contribute to our collaborative culture with honesty and integrity. At Rho, we value a strong team spirit highlighted by loyalty, accountability, and mutual trust. We work smart together, we work hard together, and we laugh together. We take responsibility for our actions, forgive honest mistakes and respect one another.
• Critical Thinker: Rho values thinking. Draw on your native ingenuity, sharpened and enhanced by our intellect, training, and experience. We evaluate situations and opportunities objectively and incisively; we then craft novel, practical solutions.
• Agile and Adaptable: Rho values the ability to change quickly. We eagerly anticipate, respond to, and take advantage of changes in our environment. We embrace risk but manage it by planning, accepting, and learning from both failures and successes. The opportunity to adapt and evolve energizes us.

Please submit your CV in English

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