Freelance Regional Clinical Trial Manager

3 dni temu

Warszawa, Mazovia, Polska Rho, Inc. Pełny etat
Overview

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 Clinical Project 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.

Responsibilities
  • 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 perform their tasks 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
Qualifications
  • 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.
  • 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.

A few more things to know about us:

Benefits: Rho provides a comprehensive benefits package for all benefit-eligible employees, and generous paid time off, holidays, parental leave and bereavement leave.

Flexibility: We encourage a work-life balance that allows employees to bring their best selves to work while being passionate about their lives outside work.

Please submit your CV in English.

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