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Full time
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gcp clinical trial ich guidelines site management regulatory

πŸ“‹ Description

  • Manage the site start up process through development of an activation readiness strategy to enable
  • Coordinate, develop and present critical path planning including IRB/EC & CA/MoH Strategy, ICF
  • Collaborate and communicate with stakeholders to secure input for milestone planning, and alignment
  • Participate in client meetings to establish client expectations for delivery, communication, risk
  • Partner closely with Functional Leaders and Site Start up Specialists to proactively identify risks
  • Provide oversight to ensure accuracy and completeness of tracking and systems are maintained in

🎯 Requirements

  • Bachelor's degree in life sciences or related field, or Registered Nurse (RN) or equivalent
  • 5 years or more in start up, ideally with SU Lead or PM experience in either a CRO or
  • 2 years or more experience in project milestone management, managing resources, budgets and
  • Demonstrated leadership experience in driving cross-functional activities.
  • Excellent communication and organizational skills.
  • Experience using computerized information systems, electronic spreadsheets, word processing and

🎁 Benefits

  • The disclosed range estimate has not been adjusted for the applicable geographic differential
  • This role is eligible for a discretionary annual bonus, health insurance, retirement savings
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