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 . Together, we create the best strategies that are both clinically relevant and scientifically meaningful . We strive to improve our knowledge of this complex disease and the vast array of available treatments in a fast-innovative way .
At MEDSIR, you will have the job of your life while working together towards our shared mission bringing novel treatments to cancer patients worldwide. 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
ABOUT THE OPPORTUNITY
IMPORTANT REQUIREMENT
- Signed agreement with your academic centre MANDATORY
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.
HOW YOU WILL CONTRIBUTE
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.
- Ensure that all deliverables are in accordance with applicable reg