TFS HealthScience is a global, mid-sized contract research organization (CRO) partnering with biotechnology and pharmaceutical companies across the full clinical development lifecycle. Our expertise spans full-service clinical development, project-based support, strategic resourcing, and Functional Service Provider (FSP) solutions, matching experienced professionals to roles where they deliver the greatest impact.
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) partnering with biotechnology and pharmaceutical companies throughout the entire clinical development journey. Our expertise spans full-service capabilities, resourcing, and Functional Service (FSP) solutions.
In this role, you will play a key part in the operational execution of Phase II and III clinical studies, contributing to the safe, effective, and responsible development of new therapies, with a strong focus on oncology trials.
Independently plan, conduct, and follow up on pre-study, site initiation, routine monitoring, and close-out visits, both on-site and remotely, in line with the monitoring plan
Oversee study site performance, including recruitment progress, and support sites with study-related questions and operational challenges within Phase II–III trials
Review eCRF data, timelines, and queries; identify and report protocol deviations; and maintain clear communication with project management and sponsors
Maintain and review study documentation at site level, including Investigator Site Files (ISF), ensuring inspection readiness and compliance with applicable regulations
Collaborate cross-functionally with medical, project management, quality, and data management teams, and support sites during audits and inspections
Degree in a scientific or medical discipline, or relevant vocational training in healthcare
Several years of experience as a Clinical Research Associate, with solid hands-on experience in Phase II and III clinical trials
Oncology experience is highly preferred
Strong knowledge of GCP, ICH guidelines, and clinical research processes, with high attention to detail in managing study data and regulatory requirements
Fluent German and English, both written and spoken, with willingness to travel nationally and internationally
We offer opportunities for both personal and professional growth in a collaborative and rewarding environment. You will join a team that values quality, teamwork, and making a meaningful impact on patients’ lives.
Our core values — Trust, Quality, Passion, Flexibility, and Sustainability — guide how we work and interact. They foster collaboration, innovation, and a shared commitment to excellence.
Founded over 30 years ago in Lund, Sweden, TFS HealthScience has grown into a global, full-service CRO. With more than 600 professionals across 50+ countries, we deliver tailored clinical research solutions across key therapeutic areas, including Oncology, Dermatology, Neuroscience, and Ophthalmology.