Clinical Trial Protocol Writer (Barcelona)

Clinical Trial Protocol Writer (Barcelona)

09 ago
|
MEDSIR
|
Barcelona

09 ago

MEDSIR

Barcelona

WHY CHOOSE MEDSIR

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

As a CLINICAL TRIAL PROTOCOL WRITER you will develop/revise the design of clinical trial proposals and protocols, and contribute with the scientific estimates to the high-level execution plan for the new projects.



You will be involved in projects under development and until they are ready for execution in hospitals worldwide, contributing both in the scientific and clinical development and in the medical writing of it.

HOW YOU WILL CONTRIBUTE:

· Responsible for generating and/or reviewing scientific documents required as part of 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, informed consent forms and other trial-specific documents that require a specialized scientific and medical knowledge. Responsibility might result in direct involvement in the preparation of those documents or supervision of outsourced activities.

· Responsible for identifying and providing the key scientific and clinical assumptions that impact on the project plan and budget.

· Ensure that all deliverables are i

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

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