Biomedical Analyst

Would you like to contribute to the development of tomorrow's pharmaceuticals and medical devices? We continue to expand our operations and are now seeking a biomedical analyst for our research clinics. As a biomedical analyst with us, you'll have a varied role that combines practical laboratory work with responsibility for developing and ensuring quality in our processes. You work both independently and together with colleagues in clinical study teams, with many contact points both internally and externally. The work is a combination of independent and routine tasks, involving frequent contact with people both inside and outside the organization: - Practical laboratory work in studies - Training clinic staff in laboratory procedures - Responsible for equipment operation and maintenance as well as organization and structure in the laboratory environment - Protocol review - Contributing to internal development and quality work by writing and updating manuals and instructions - Practical study-related tasks such as sample collection, sample handling, ECG, blood pressure, pulse Who we are looking for Requirements - Educated biomedical analyst or equivalent - Previous experience with laboratory work - Good ability to express yourself in Swedish and English, both orally and in writing Meritorious - Previous experience with clinical trials or research Personal qualities We are looking for someone who is a careful person who values delivering optimal quality within agreed timeframes. You have an easy time collaborating and building relationships and enjoy working on multiple projects in parallel. We particularly value that you: - Have high service awareness and actively contribute to the clinical study team from start to finish - Have a professional and respectful approach to sponsor, clinic, subcontractors, and colleagues - Have the ability to adapt when circumstances change - As an employee at CTC, it is also natural that you share our values: Innovation, Community, Respect, Commitment, Professionalism – iGREP Other information Permanent position with 6-month trial employment. Full-time position. Start date by agreement. Work is mainly conducted on weekdays during daytime, but evening and weekend shifts may occur. Work location: Uppsala At CTC you get to 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. We look forward to reading your application and telling you more about what it's like to work with us. Application deadline: September 21, 2026. Recruitment is ongoing, which means the position may be filled before the final application deadline. 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, tasks, and deliverables required to conduct a clinical trial – all so that new pharmaceuticals and medical devices reach patients as quickly as possible. We currently 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 have approximately 125 employees, about half of whom work clinically. Our headquarters are located in Uppsala.

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