Specialist/Snr Specialist Study Start Up and Regulatory Affairs

Added
1 day ago
Type
Full time
Salary
Salary not provided

Related skills

documentation regulatory affairs ssu ich-gcp regulatory strategy

๐Ÿ“‹ Description

  • The Senior Specialist, Study Start Up and Regulatory Affairs leads and coordinates all activities
  • Provides subject matter expertise, ensures regulatory compliance, and serves as a key liaison with
  • Accountable for delivery of assigned study start-up and regulatory milestones within defined scope.
  • Make independent decisions regarding regulatory processes and documentation approaches.
  • Handles medium-complexity regulatory environments, including multi-country requirements where
  • Leads study start-up and regulatory activities for assigned countries or projects, ensuring timely

๐ŸŽฏ Requirements

  • Graduate degree in Chemistry or Life Sciences, Nursing or equivalent combination of education and
  • Minimum 4 years within pharmaceutical or CRO industry or regulatory body
  • Good knowledge of ICH GCP and national regulations for territories of competency
  • Good understanding of country requirements pertaining to SSU/Regulatory delivery in multiple

๐ŸŽ Benefits

  • We look forward to welcoming your application and offer a collaborative, international team
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