Freelance Clinical Research 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 Freelance Clinical Research Associate (0.2 FTE) - home based in Portugal. Whilst this opportunity is for 0.2 FTE, we may require you to work up to 0.3 FTE during some periods. This contract is for 1 year. Prior experience in either Urology or Overactive Bladder is required. About this role As part of our Internal Medicine and Neuroscience team you will be working alongside passionate and innovative professionals to ensure our customers achieve their goals. The Freelance Clinical Research Associate is part of Clinical Development Services (CDS) within TFS HealthScience, will function operationally as a member of a Project Team and is responsible for the initiation, on-site and/or remote monitoring and close out of study sites during study conduct, according to company policies, SOPs and regulatory requirements. Key Responsibilities: - Monitor on-site and remotely clinical trials in accordance with TFS and/or sponsor Standard Operating Procedures GCP and ICH guidelines and applicable regulatory regulations. - Perform all required monitoring activities at the study sites to assess and ensure subjects safety, data integrity and quality. - Verify the protection of study participants by informed consent procedures and protocol requirements that follow appropriate regulations. - Review CRFs (electronic or paper) and subject source documentation for validity and accuracy - Verify proper management and accountability of Investigational Product. - Timely reporting of actions taken during monitoring visits in Monitoring Visit Report including findings, corrective and preventive actions already taken and update