At a Glance
- Tasks: Prepare clinical trial applications and ensure compliance with regulations.
- Company: Medpace is a leading Clinical Operations team based in London.
- Benefits: Enjoy flexible PTO and a competitive compensation package.
- Other info: Proficiency in Microsoft Office and excellent organizational skills are essential.
- Why this job: This role offers structured career growth opportunities in a dynamic environment.
- Qualifications: A Bachelor’s degree in Life Sciences and experience in regulatory documentation are required.
The predicted salary is between 30000 - 40000 £ per year.
Medpace is seeking an experienced Regulatory Submissions Coordinator to join our Clinical Operations team in London. This key position involves preparing clinical trial applications and ensuring compliance with regulations.
A Bachelor’s degree in Life Sciences and prior experience in regulatory documentation are required. The role requires excellent organizational skills, attention to detail, and proficiency in Microsoft Office.
Medpace offers a competitive compensation package and employee wellness initiatives.
Regulatory Submissions Coordinator - London | Flexible PTO employer: Medspace
Medpace, located in London, provides a flexible work environment and prioritises employee wellness initiatives. The Clinical Operations team focuses on ensuring compliance and excellence in clinical trials.
