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Senior Clinical Trial Specialist

Tandym Group

A pharmaceutical company in Massachusetts is looking to add a new Senior Clinical Trial Specialist to join their team in Bedford, providing logistical support for clinical trials in collaboration with cross-functional teams to ensure compliance with operational procedures and regulations.

About the Opportunity:

  • Schedule: Full-time
  • Hours: Standard business
  • Setting: Varied clinical environments
Responsibilities:
  • Managing regions/sites and CRO under the direction of a Study Lead
  • Overseeing vendors, contracts, and financial forecasting
  • Developing and maintaining study documents
  • Contributing to the Study Management Team meetings
  • Reviewing the Trial Master File and updating documents
  • Performing other duties, as needed
Qualifications:
  • 4 years of Clinical Research experience
  • Bachelor's Degree in Healthcare and/or a Scientific-related field
  • Solid understanding of Study Phases
  • Solid problem-solving and time management skills
  • Ability to handle multiple tasks and deadlines
Desired Qualifications:
  • Master's Degree
  • Certification such as CCRP
  • Advanced skills in Project Management
Vacancy posted 1 day ago
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