Added
16 hours ago
Type
Full time
Salary
Salary not provided

Related skills

gcp ich guidelines regulatory submissions clinical trial services irb/ec
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πŸ“‹ Description

  • Manage the site start up process
  • Coordinate, develop and present critical path planning
  • Collaborate and communicate with stakeholders for milestone planning
  • Participate in client meetings
  • Provide oversight to ensure accuracy and completeness of tracking and systems
  • Coordinate translations for documents required for submissions

🎯 Requirements

  • Bachelor's degree in life sciences or related field, or Registered Nurse (RN) or equivalent
  • 5+ years in start up, ideally with SU Lead or PM experience in CRO/pharma/biotech
  • 2+ years in project milestone management, managing resources, budgets, coordinating team activities
  • Demonstrated leadership in cross-functional activities
  • Excellent communication and organizational skills
  • Experience with computerized information systems, spreadsheets, word processing, email
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