Join leading oncology departments in Ireland

Are you a pathologist and would like to work and live on Norway’s beautiful west coast? Then we would love to hear from you. We are looking for a specialist in pathology for a permanent 100% position at a hospital on Norway’s beautiful west coast. This is an excellent opportunity for a pathologist who wants to work in a strong professional environment with varied and meaningful diagnostic work. The department plays an important role in patient diagnosis and treatment, working closely with clinical teams across the hospital. You will join a committed and experienced team with a broad diagnostic scope and a strong focus on professional development. Responsibilities Histological and cytological diagnostics. Participation in autopsies and, where relevant, frozen section work. Collaboration with clinical departments and multidisciplinary teams. Contribution to internal teaching, quality improvement, and professional development. Helping further develop the department’s diagnostic work. Qualifications European medical licence and specialist approval in pathology. Experience in histology and cytology is desirable. Strong collaboration and communication skills. Fluent English skills and willingness to learn Norwegian. We offer A permanent position in a solid professional environment. Varied work and broad diagnostic experience. A supportive and inclusive working atmosphere. Good opportunities for professional growth and development. As part of the recruitment process, we provide: Free online language training with a private tutor Assistance with authorisation and relocation Support for you and your family throughout the entire process The phrase “Norway’s beautiful west coast” is well supported as a natural promotional description of the region, which is known for its fjords, mountains, and coastline. Interested in learning more? This is an excellent opportunity for pathologists who would like to broaden their international experience while working in a modern European hospital setting. Feel free to get in touch for more information about the hospital, location, and practical details to help you evaluate whether this opportunity could be the right fit for you.

ABOUT THIS ROLE 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 Provider (FSP) solutions. We are currently looking for a Clinical Study Coordinator to support an ongoing multicentre clinical trial during a high-intensity enrollment period. This is a hands-on, site-based role focused on patient identification, visit coordination, and operational trial support within hospital environments where timely patient enrollment is critical. As part of our Strategic Resourcing Solutions (SRS) team, you will be dedicated to a leading global biopharmaceutical company. This is a freelance consulting assignment with an expected commitment of approximately 50% (0.5 FTE) for an initial six-month period. KEY RESPONSIBILITIES * Maintain regular on-site presence to identify and track potentially eligible patients across relevant hospital departments. * Coordinate participant enrollment and study visits within protocol-defined timelines. * Manage visit schedules and ensure all study-related activities occur within required visit windows. * Complete source documentation and data entry in accordance with ICH-GCP, protocol requirements, and sponsor standards. * Collaborate closely with investigators, research staff, and hospital personnel to support day-to-day study conduct. * Act as a key operational link between site teams and sponsor stakeholders. * Support screening, recruitment, and patient flow activities during peak enrollment periods. * Ensure accurate study documentation and timely communication across all involved parties. QUALIFICATIONS * Degree in Nursing, Life Sciences, Pharmacy, Biomedical Sciences, or a related field. * Previous experience as a Study Coordinator, Clinical Research Coordinator, Research Nurse, CRA, or similar clinical research role. * Strong understanding of ICH-GCP and clinical trial processes. * Experience working within hospital, clinical, or research environments. * Excellent organizational skills with the ability to manage multiple priorities in a fast-paced setting. * Strong communication and stakeholder management skills. * Fluency in Swedish and English, both written and spoken. * Ability and willingness to work on-site at hospital locations in Southern Sweden. PREFERRED QUALIFICATIONS * Previous involvement in multicentre clinical trials. * Experience with EDC systems and clinical trial data entry. * Familiarity with patient recruitment and enrollment activities. WHAT WE OFFER 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. In this role, you will have the opportunity to contribute directly to important clinical research while working alongside experienced professionals in a dynamic and collaborative environment. A BIT MORE ABOUT US 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.