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Senior Regulatory Affairs Associate at Park Street People
London, Essex - England, United Kingdom -
Full Time

Start Date

Immediate

Expiry Date

10 Nov, 26

Salary

55000.0

Posted On

05 Oct, 26

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Pharmaceutical Manufacturing

Description
  • Other responsibilities include:You will develop, contribute and ensure the accurate preparation of high-quality regulatory documents needed to support clinical trials and medical products.
  • Contributing regulatory guidance in order to enhance product development.
  • Ensuring that product development is aligned with the company’s strategy business model as well as global regulatory requirements.
  • Acting as a point of contact between the company and regulatory agencies whilst pertaining important information.


  • RequirementsPrevious experience in Regulatory Affairs and Compliance particularly within pharmaceutical industry.
  • You will have a proven background working on CTAs (clinical trial application) and MAAs (marketing authorisation application)
  • Exposure of Regulatory Affairs legislation and procedures
  • Strong communication and interpersonal skills

How To Apply:

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Responsibilities