Job Summary:
This role is focused on the creation of clinical study protocols, ensuring that all necessary information is accurately documented and communicated to stakeholders. The ideal candidate will have a strong background in life sciences, excellent communication skills, and the ability to manage project timelines effectively.
About the Role:
* The primary responsibility of this position is to prepare clinical study protocols, which involves researching and documenting scientific information related to the development of new medical treatments.
* Additional responsibilities include managing project timelines, conducting customer meetings, and ensuring that all projects are completed within set deadlines.
Requirements:
* Bachelor's degree in life sciences
* Minimum 3 years of experience in medical writing
* Strong attention to detail and excellent communication skills
Benefits:
This role offers an opportunity to contribute to innovative medical treatments and improve patient outcomes. With a focus on creating high-quality clinical study protocols, you will play a critical role in advancing the development of new medical treatments.