Clinical Study Manager

2 days ago


Sydney, New South Wales, Australia Pfizer Full time
About the Role

Pfizer is seeking a highly skilled and experienced Clinical Study Manager to join our team. As a Clinical Study Manager, you will be responsible for managing clinical studies from start to finish, ensuring that they are completed on time, within budget, and to the highest quality standards.

Key Responsibilities
  • Develop and implement study plans, protocols, and procedures
  • Manage and coordinate study activities, including site activation, data collection, and data analysis
  • Ensure compliance with regulatory requirements and Pfizer's policies and procedures
  • Collaborate with cross-functional teams, including clinical research, regulatory, and quality assurance
  • Provide training and support to site staff and investigators
  • Monitor and report on study progress, identifying and resolving any issues that may impact study timelines or quality
Requirements
  • Bachelor's degree in a life science or related field
  • 7+ years of experience in clinical research, with a focus on study management
  • Strong knowledge of Good Clinical Practices (GCP) and regulatory requirements
  • Excellent communication and project management skills
  • Ability to work independently and as part of a team
What We Offer

Pfizer offers a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and experienced Clinical Study Manager looking for a new challenge, we encourage you to apply.



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