Regulatory Affairs Specialist

5 days ago


Solna Municipality, Sweden Valneva Full time

Valneva is seeking an experienced Clinical Study Manager to join our team and lead the execution of clinical studies.

About the Job
  • This role requires a strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
  • Responsibilities include managing clinical research tasks, collaborating with service providers, and ensuring data quality.
  • The successful candidate will contribute to the development of core study documents, facilitate timely reporting, and collaborate with Valneva stakeholders.

Our ideal candidate has a Master's degree in Life Science or equivalent experience, preferably with 5+ years in clinical trials management. Strong organizational skills, IT proficiency, and fluency in English are essential.

Requirements
  • Completed Master's Degree in Life Science or equivalent combination of education and work experience
  • At least 5 years of experience as a Clinical Project Manager (CPM) and/or as Clinical Research Associate (CRA)
  • Experience in overseeing external service providers


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