Regulatory Affairs Associate(CMC),Contract,Global pharma,London

Our client, a well-known global company based in London, is offering an immediate start for an Associate Regulatory Affairs professional on a fixed 12-month contract basis. By joining our client, you'll have the opportunity to gain valuable industry experience in an established organization known for its contribution to the pharmaceutical sector. Our track record of successfully managing and executing regulatory CMC projects across various product development phases speaks volumes about the quality of experience you can expect.

Responsibilities:

- Collaborate with the CMC team to project manage and execute regulatory submissions
- Maintain submission timelines with precision and attention to detail
- Coordinate document reviews and other project tasks efficiently

Requirements:

- Proficient in Microsoft Office suite, especially Word, Excel, PowerPoint, and Project
- Strong organizational and time management skills
- Excellent interpersonal and communication skills
- Degree in life sciences, biochemistry, or chemistry preferred
- Experience in biopharmaceutical or pharmaceutical industry is a plus
- Familiarity with eCTD structure and CMC submissions client preferred

Benefits:

- Immediate start in a well-known global pharmaceutical company
- Fixed 1-year contract providing a focused learning experience
- Exposure to diverse CMC projects enhancing your industry knowledge

Apply now and become a part of this exciting journey!

Interested? Don't miss out on this exciting opportunity! Apply today and take your career to new heights. Send me a copy of your CV in Word format or share as this is a great opportunity for the right person! This is a 1 year contract and the client is looking for someone to start as soon as possible so please share your CV if interested, forward to Oksana at ##### or via linked in.

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