We are a Barcelona-based fastest-growing company founded by scientific experts . We are dedicated to the design and management of innovative strategic clinical trials in oncology, from study conception to the publication of study results . We welcome top performers that will bring new ideas, diverse perspectives, and provide you the opportunities and freedom to grow and make a real impact in patients' lives and science… all while having great fun The main objective of this role is to support the development and revision of the design of clinical trial proposals and protocols. As a Trainee, you will assist in various projects under development until they are ready for execution in hospitals worldwide, contributing to both the scientific and clinical development and the medical writing. As trainee you will be involved in and learn about: Assist in generating and/or reviewing scientific documents required as part of the design of new MEDSIR clinical trials or updates on existing projects. Documents might include but are not limited to synopsis of new clinical trials, protocols, and other trial-specific documents that require specialized scientific and medical knowledge. This may include direct involvement in the preparation of those documents or supervision of outsourced activities. Help identify and provide the key scientific and clinical assumptions that impact the project plan and budget. Assist in setting up new clinical trials in public registry databases (clinicaltrials.gov, EUCT, or equivalent databases). Monitor deadlines and ensure projects are delivered within agreed timelines. Stay current with medical literature and advancements by keeping abreast of current literature, emerging science, technological developments, and medical trends. Participate in scheduled company trainings.



University degree in health or life science-related field, such as Biology, Biochemistry, Biomedicine, Genetics, Biotechnology, Medicine, Pharmacy or a related discipline. Basic understanding of clinical research principles. Specific training in clinical trials, Good Clinical Practice (GCP), or related areas will be highly evaluated. Solid writing and organizational skills with meticulous attention to detail. Proficiency in computer skills, including search databases, and MS Office package or equivalent. Motivation and ability to keep scientific knowledge updated in areas required by the company projects that include but are not limited to Oncology, Molecular Biology, Digital Innovation in Health Sciences. Ability to interpret clinical data and other complex information and communicate in a clear and concise manner. Ability to communicate effectively in English and preferably in additional languages. We work to create a culture of empowerment, continuous learning and growth where everyone can bring expertise, own projects and easily measure their impact Study compensation support for basic transport and food expenses Fast growth, we are an early-stage company with a multidisciplinary team and many growth opportunities. Work-life balance - hybrid working model and versátil hours focusing on performance rather than office hours. Unlimited access to GoodHabitz courses and regular workshops (external & internal) to continue your development. Opportunities to participate in scientific conferences & events at national and international level. Work-from-abroad policy depending on position and local legislation. A young & international team with a company culture focused on development. Unforgettable MEDSIR events and regular get togethers. We work with MacBook computer (Apple).

📌 Trainee Clinical Trial Protocol Writer (Barcelona)
🏢 MEDSIR
📍 Barcelona