Logo

Clinical Project Manager

Upsilon Global, Healthcare, Belgium

Upsilon Global, a leading clinical research organization in Belgium, specializing in rare disease studies such as Cystic Fibrosis, is currently seeking a dedicated Freelance Project Manager to oversee a groundbreaking Rare Disease Clinical Study. We are committed to ensuring the highest standards of quality and compliance with local and international regulations in all our research endeavors. At Upsilon Global, we value collaboration, innovation, and excellence in everything we do.

As the Project Manager for this exciting opportunity, you will play a crucial role in managing all aspects of the study from start-up to close-out. Your responsibilities will include overseeing clinical trial execution, ensuring adherence to timelines and budgets, managing regulatory submissions and ethics committee documentation, monitoring site activation and patient recruitment progress, collaborating with sponsors, investigators, and regulatory bodies, identifying risks, implementing mitigation strategies, and providing leadership to clinical teams throughout the study process.

The ideal candidate for this position will have at least 5 years of project management experience in clinical research, preferably with a background in rare disease trials. A strong understanding of Belgian and EU regulatory requirements is essential for success in this role. Additionally, excellent leadership skills along with effective communication and problem-solving abilities are key attributes we are looking for. Fluency in English is required to effectively communicate with stakeholders across different regions.

If you are passionate about making a difference in the field of rare diseases through innovative research projects and possess the necessary skills and experience outlined above, we invite you to apply for this rewarding opportunity at Upsilon Global. This position is ideal for experienced Project Managers looking to take on new challenges within the realm of rare disease clinical studies. Join us in our mission to advance medical knowledge and improve patient outcomes through cutting-edge research initiatives. Contact Amani Manaka or call +44 203 875 9966 today for more details on how you can become part of our dynamic team.

Key Job Requirements:
  • 5+ years of project management experience in clinical research
  • Experience in rare disease trials
  • Strong understanding of Belgian and EU regulatory requirements
  • Fluency in English
Key Job Responsibilities:
  • Oversee clinical trial execution
  • Manage regulatory submissions and ethics committee documentation
  • Monitor site activation, patient recruitment, and study progress
  • Collaborate with sponsors, investigators, and regulatory bodies
Skills:
  • Project management
  • Clinical research
  • Regulatory compliance
  • Leadership skills
  • Communication skills

Seniority Level: Middle Management

  • Senior Level

Job Functions: Project Management

  • Clinical Research
  • Regulatory Affairs

Industries : Healthcare

  • Pharmaceuticals
  • Biotechnology

More Clinical Research , Regulatory Affairs jobs in Belgium

CV Drop Zone

  • Drag your CV in supported formats such as pdf, doc, and docs.
  • Register for real-time updates on your application status.
  • Your CV becomes readily available for download by the employers.
  • You acknowledge and agree to OWCareers' terms, conditions, and privacy policies.
  • Optimize your application by providing comprehensive and accurate information.
  • Explore additional resources on our platform to refine your resume.

Contact Job Poster