Clinical Trial Associate (Temporary - 6 months, 1FTE)

Job description

About this role TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions. The Clinical Trial Associate (CTA) is part of the Clinical Operations or Strategic Resourcing Solutions Unit within TFS Develop and will work, when delegated, as a member of the study team with the responsibility to organize and maintain the Study Master File (SMF) and coordinate practical tasks during the study according to company policies, SOPs and regulatory requirements. Key Responsibilities: Work with the Study Team in initiating, maintaining and closing/final archiving of the SMF ensuring GCP compliance Set up and maintenance of study information in Clinical Trial Management System (CTMS) as per delegation from PM/ Lead CRA or CRA Maintenance of electronic files: Set up the Investigator’s File as directed by the CRA Point of contact regarding SMF: Maintain the SMF as directed by the Lead CRA/Project Manager Coordinate study supplies as directed by the CRA Drafts...