At a Glance
- Tasks: Lead the review of essential clinical documents and collaborate with senior leaders.
- Company: Join a top global pharmaceutical company in a dynamic London setting.
- Benefits: Competitive pay, hybrid work model, and opportunities for professional growth.
- Other info: 12-month contract with a chance to work in a collaborative environment.
- Why this job: Make a significant impact in the pharmaceutical industry while enhancing your project management skills.
- Qualifications: Bachelor’s in Life Sciences and 5+ years in pharma with strong project management experience.
The predicted salary is between 60000 - 75000 £ per year.
PE Global (UK) is recruiting for a Clinical Document Review Lead on behalf of a leading global pharmaceutical company in London. This role requires overseeing the review of critical clinical development documents while working collaboratively with senior clinical leaders and cross-functional teams.
The ideal candidate will have a Bachelor’s degree in Life Sciences, along with at least 5 years of experience in the pharmaceutical industry and strong project management skills.
The position is a 12-month hybrid contract, offering a competitive rate.
Clinical Document Review Lead — Hybrid, London employer: PE Global (UK)
PE Global (UK) is an exceptional employer, offering a dynamic work environment in the heart of London where innovation meets collaboration. Employees benefit from a competitive salary, flexible hybrid working arrangements, and ample opportunities for professional growth within a leading global pharmaceutical company. Join us to be part of a supportive culture that values your contributions and fosters career advancement in the ever-evolving field of clinical development.
