At a Glance
- Tasks: Create and manage clinical study documents while ensuring top-notch quality and compliance.
- Company: Meeveem Limited, a forward-thinking company in the pharmaceutical industry.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Work in a collaborative environment with a focus on scientific excellence.
- Why this job: Join a dynamic team and contribute to impactful medical research.
- Qualifications: 2+ years of medical writing experience and strong project management skills.
The predicted salary is between 40000 - 50000 £ per year.
Meeveem Limited seeks a Medical Writer to develop and manage clinical study documents, ensuring high-quality and regulatory compliance. The ideal candidate has at least 2 years of medical writing experience in the pharmaceutical industry and possesses excellent project management and communication skills.
This role is hybrid, requiring attendance in the London office for at least 2 days per week. A Bachelor’s degree or equivalent in a scientific field is preferred to support scientific documentation goals.
Medical Writer - Regulatory & Study Documentation in London employer: Meeveem Limited
Meeveem Limited is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for Medical Writers looking to make a meaningful impact in the pharmaceutical industry. With a strong emphasis on employee growth and development, we offer comprehensive training opportunities and support for career advancement, all while enjoying the vibrant atmosphere of our London office. Our hybrid working model ensures flexibility, allowing you to balance your professional and personal life effectively.
