Freelance 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.

We are currently seeking a Clinical Trial Associate (CTA) to support the successful execution of clinical studies within a biotechnology this role you will play a key part in maintaining clinical trial documentation ensuring eTMF quality and compliance and supporting the day-to-day coordination of study activities.

As part of our SRS/FSP team you will be dedicated to one sponsor a biotechnology company at the forefront of innovation within oncology research.

• Prepare organize maintain and archive essential clinical trial documentation

• Manage and maintain the eTMF ensuring completeness quality and inspection readiness

• Support document management activities including DocuSign administration and R&D archiving

• Coordinate study meetings site visits and communication between sites vendors investigators and internal study teams

• Prepare meeting materials presentations agendas and meeting minutes

• Support study tracking activities and maintain information in CTMS and EDC systems

• Assist with ethics submissions regulatory documentation and study amendments

• Support operational study activities including planning and budget tracking

• Ensure documentation complies with GCP company SOPs and applicable regulatory requirements

• Support audit and inspection readiness activities

• Bachelors degree in Life Sciences Pharmacy Nursing or a related field

• Previous experience as a Clinical Trial Associate Clinical Trial Coordinator Study Coordinator or similar clinical operations role

• Hands-on experience with eTMF management and clinical trial documentation

• Experience working with CTMS EDC systems and Microsoft Office applications

• Strong knowledge of GCP and ICH-GCP guidelines

• Excellent organizational and communication skills

• Fluent in English and Swedish both written and spoken

• Initial 12-month assignment

• Approximately 0.5 FTE

• Planned start in October

• Lund Sweden

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.

Our journey began over 30 years ago in Sweden in the city of Lund. As a full-service global CRO we build solution-driven teams working toward a healthier future. Bringing together over 600 professionals TFS delivers tailored clinical research services in more than 50 countries offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology Neuroscience Oncology and Ophthalmology.