Senior Clinical Trial Specialist

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