Clinical Research Nurse

Do you want to be an important part of our continued journey, where we contribute to the future of healthcare through clinical studies? Do you enjoy combining patient-centered work with administration and appreciate a varied work day at an innovative employer? Then the role of Clinical Research Nurse at CTC might be for you! As a Clinical Research Nurse at CTC, you will be responsible for some of our clinical research studies. This means you will plan, coordinate the initiation and practical implementation of studies in accordance with given regulations and requirements. You will also be responsible for contact with our external clients and collaborative partners. You will work in close collaboration with other clinical research nurses, physicians, and research nursing assistants where you all contribute your expertise in an environment that offers opportunities for personal development. In the clinical care of research participants, you will handle tasks such as specimen management, medication handling, and collection of clinical parameters such as ECG and blood pressure. You will also be responsible for data management such as e-CRF and other study-related systems and documents. Who are you? We are looking for someone who preferably has previous experience with similar work. As a person, you are driven, solution-focused, and not afraid to try new tasks. You have a positive attitude, are social and professional in your interactions with colleagues, clients, and research participants. You are responsible and enjoy working both independently and as part of a team with others. Being thorough and organized is essential, and you appreciate working in a fast-paced and changing environment. As an employee with us, we offer you an organization with short decision-making processes where we help each other with our ambition to develop methods to streamline the implementation of clinical studies. As an employee, you are covered by a collective agreement and we encourage work-life balance by offering, among other things, flexible working hours, health and wellness benefits, and generous vacation terms. As an employee at CTC, it is also a given that you share our core values of Innovation - Community - Respect - Commitment - Professionalism, iGREP. Requirements Licensed Registered Nurse Minimum 5 years of work experience Speak and write Swedish fluently and have good knowledge of English Meritorious Previous experience working as a Clinical Research Nurse Other Information Full-time or by agreement. Work is mainly scheduled for weekdays during daytime, but evening and weekend shifts may occur. We prefer that you work full-time (100%) as it provides good continuity in studies and the opportunity to develop quickly in the role, but we are open to discussing a part-time arrangement. Location: Uppsala Does this sound like a role for you? At CTC, you will work in an organization where quality, commitment, and collaboration are in focus. We offer a stimulating and developing work environment where you have the opportunity to contribute to research that makes a difference. I look forward to reading your application and telling you more about what it's like to work with us. Alexandra Pallas Recruitment Manager [email protected] 0730-758794 Application deadline is through September 21, 2026. Recruitment is ongoing, which means the position may be filled before the final application date. Start date by agreement. About the Employer - CTC Clinical Trial Consultants AB CTC Clinical Trial Consultants AB is a Clinical Research Organisation (CRO) with operations in Uppsala, Stockholm, Linköping, and Gothenburg. CTC is a wholly-owned subsidiary of Center for Translational Research AB, which is also the parent company of Zelmic, TKT, RegSmart, Lablytica, MetaSafe, and CTC Netherlands. Together with our sister companies, we deliver a comprehensive solution to our customers for the development of clinical products. As a CRO, we conduct clinical studies on behalf of industry and academia and offer a complete full-service package that includes the services, activities, and deliverables required to conduct a clinical trial – all to get new drugs and medical devices to patients as quickly as possible. Today we conduct studies from early to late phase (phase 0-IV). Studies are conducted primarily at our own research clinics, but we also collaborate with external clinics. We employ approximately 125 employees, of whom about half work clinically. Our headquarters is located in Uppsala.

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