Clinical Research Associate

We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference.

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.

We are seeking a Clinical Research Associate (CRA) to support the successful delivery of clinical trials across designated sites. In this role, you will be responsible for ensuring patient safety, data quality, protocol compliance, and strong site performance while taking ownership of site management activities and building effective relationships with investigators and site staff.

As part of our Functional Solutions team, you will be dedicated to one sponsor, a global pharmaceutical company that is an industry leader within its therapeutic area.

• Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols, ICH-GCP, and applicable regulations

• Ensure subject safety, data integrity, and protocol compliance throughout the study lifecycle

• Build and maintain strong relationships with investigators, study coordinators, and site personnel

• Identify, document, and proactively resolve site issues, risks, and recruitment challenges

• Complete monitoring reports and maintain accurate study documentation and trial management systems

• Collaborate with project teams and stakeholders to ensure study milestones and deliverables are achieved