Clinical Trial Associate Job at TFS HealthScience | Apply Now
A Clinical Trial Associate Job at TFS HealthScience is available in Lund, Sweden, supporting clinical studies within a biotechnology environment, with an initial assignment planned to start in October.
- Position: Clinical Trial Associate (CTA)
- Location: Lund, Sweden
About TFS HealthScience
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. The organization offers full-service capabilities, resourcing, and Functional Service (FSP) solutions, ensuring high-quality support for clinical trials.
Clinical Trial Associate Job Description
In this Clinical Trial Associate Job, the successful candidate will play a key role in maintaining clinical trial documentation, ensuring eTMF quality and compliance, and supporting the day-to-day coordination of study activities. This position is dedicated to one sponsor, a biotechnology company at the forefront of innovation within oncology research.
Eligibility Criteria
- Bachelor’s degree in Life Sciences, 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.
Clinical Trial Associate Job – Key Responsibilities
- 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.
Why Join TFS HealthScience?
TFS HealthScience provides opportunities for personal and professional growth in a rewarding environment. The organization values collaboration, quality, and making a difference in the lives of patients. Their core values of Trust, Quality, Passion, Flexibility, and Sustainability guide their decisions and shape their culture, fostering innovation and a shared commitment to excellence.
This Clinical Trial Associate Job is a compelling opportunity for qualified candidates to contribute to innovative clinical studies at TFS HealthScience. Interested candidates should apply before the planned start in October to ensure their consideration for this role.
