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Clinical Project Oversight Specialist

1 tydzień temu

Warszawa, Mazovia, Polska Tomasz Rutkowski Solo Law Firm Pełny etat
About the Ideal Candidate

We are seeking a highly experienced professional with at least 15 years of industry experience and a minimum of 5 years at a CRO. The ideal candidate will have a strong background in clinical project management, including management of all phases of clinical trials from start-up to closure.

The ideal candidate will also have experience leading concurrent multi-centered, multinational phase III clinical trials, including project budget financial tracking and forecasting. Additionally, the ideal candidate will have substantial experience in project supervision, mentoring, and coaching project managers.

We are looking for a professional who can demonstrate a strong understanding of good clinical practices, applicable Health Canada and FDA regulations/guidelines, and who can apply study-specific learning across assigned portfolio of studies/clients.

  • Requirements:
  • Bachelor of Science in a relevant discipline.
  • A Master's degree is an asset.
  • PMP or PRINCE2 Certification is an asset.
  • At least 15 years industry experience and a minimum of 5 years at a CRO.
  • At least 10 years of clinical project management experience, including management of all phases of clinical trials from start-up to closure.
  • Experience leading concurrent multi-centered, multinational phase III clinical trials, including project budget financial tracking and forecasting.
  • Substantial experience in project supervision, mentoring, and coaching project managers.
  • Good knowledge of good clinical practices, and applicable Health Canada and FDA regulations/guidelines.