Statistician in Clinical Trials

CTC Clinical Trial Consultants AB · Full-time

Dag Hammarskjölds väg 10B, UPPSALA, Sweden

Do you want to use your statistical expertise to contribute to the development of future medications and medical devices? CTC is now seeking a Biostatistician for the Biometrics department in Uppsala, where eCRF Managers and statistical programmers also work. In this role, you will contribute statistical expertise throughout the study, from planning and selecting analysis methods to analyzing, interpreting, and reporting results. In this role, you will work both independently and in close collaboration with colleagues in the Biometrics team, other professionals in the clinical study teams, and with our clients. Your main responsibilities are to: Provide statistical input to study protocols, eCRF (data entry forms), and study reports. Take responsibility for selecting statistical analysis methods and randomization procedures. Write statistical analysis plans (SAP). Program statistical analyses in SAS in accordance with study protocols and SAP, and conduct statistical analysis of clinical study data. Contribute to the further development of statistics and programming-related processes and templates. Participate in client meetings as a statistical expert during planning, execution, and follow-up. Who we are looking for We are looking for someone who is meticulous and quality-conscious and takes responsibility for delivering high-quality work within agreed timelines. You drive work forward independently while also seeking support and anchoring questions when needed. When you encounter problems, you work methodically to understand the cause, evaluate different options, and find a working solution. Because this role has many contact points, you need to be able to translate needs between different professions and build constructive collaboration. With a service-oriented approach, you try to understand what colleagues and customers need and how you can help them move forward. You communicate clearly and professionally and adapt explanations so that even people without a statistical background can understand the reasoning and results. We also value that you share CTC's core values: Innovation, Community, Respect, Commitment, and Professionalism – iGREP. Requirements: Academic degree in statistics or mathematical statistics Good knowledge of database modeling and data management Experience with SAS programming Good ability to express yourself in Swedish and English, both verbally and in writing. Merits: Experience working as a statistician in clinical trials and/or medical research. Experience with clinical trials and knowledge of Good Clinical Practice (GCP) What we offer At CTC, you have the opportunity to work close to the entire clinical study chain in a knowledge-intensive organization with short decision-making processes and a vibrant culture. We help each other, share knowledge, and leverage each other's strengths. With clear goals, trust, and shared commitment, we contribute to new medications and medical devices reaching patients. We offer collective agreements with associated insurance packages, as well as wellness contributions, wellness hours, and flexible working hours to help you balance your life. The role is based in Uppsala. During the introduction, you will work on-site; thereafter, there is an opportunity for hybrid work up to two days per week based on the needs of the business and projects. Application This is a permanent full-time position with a 6-month trial period. Start as soon as possible by agreement. Selection and interviews are ongoing, which means the position may be filled before the application deadline. Therefore, do not delay your application. If you have questions about the position, please contact the recruiting manager: Eva Jacobsson, 070-271 31 49, [email protected] We look forward to learning more about you and what you can bring to our team! This recruitment is handled entirely by CTC. We therefore decline calls from recruitment companies and advertising sales. 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 complete 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, processes, and deliverables required to conduct a clinical trial – all to help new medications and medical devices reach patients as quickly as possible. We currently conduct studies from early to late phase (phases 0-IV). Studies are conducted primarily at our own research clinics, but we also collaborate with external clinics. We have approximately 125 employees, of whom about half work clinically. The head office is located in Uppsala.