Clinical Trial Associate

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.Join Our Team as a Clinical Trial Associate (CTA)About this roleAs part of our Strategic Resourcing Solutions (SRS) team you will be working alongside passionate and innovative professionals to ensure our customers achieve their goals.The CTA is responsible for organizing and maintaining the Study Master File (SMF) and coordinating 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.Qualifications:Bachelor's Degree preferred.Knowledge of GCP/ICH guidelines.Good written and communication skills.Good organizational skills.Good software and computer skills.Able to work in a fast-paced environment with changing priorities.What We OfferWe provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You'll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.
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