Clinical Trials Specialist

3 days ago

Slough, Slough, United Kingdom CK Group Full time
Job Description

CK Group is seeking a highly skilled Clinical Trial Associate to join our team on a contract basis. This role is an excellent opportunity for a motivated individual to work with a global pharmaceutical company based in Slough.

Key Responsibilities:
  • Develop and Maintain Trial Master Files (TMFs): Create and implement TMF plans, conduct ongoing and final quality control checks to ensure compliance.
  • Support Audit and Inspection Activities: Collaborate with the Clinical Development Quality Lead to ensure seamless audit and inspection processes.
  • Subject Matter Expertise: Provide expert knowledge on client systems and identify opportunities for process improvements between client and partner systems.
  • Participate in Clinical Study Team Meetings: Contribute to trial-related discussions and provide expertise as required.
Requirements:
  • Relevant Scientific Degree or Equivalent Experience: Hold a degree in a relevant scientific field or have equivalent working experience.
  • Previous Experience in Creating TMFs: Proven track record of creating high-quality TMFs in the pharmaceutical industry.
  • Excellent Communication and Attention to Detail: Possess excellent communication skills and a keen eye for detail.
About Our Client

Our client is a global biopharmaceutical company dedicated to creating value for people living with severe diseases in immunology and neurology. They are committed to delivering innovative solutions and improving patient outcomes.

Location

This role is based at our client's site in Slough, providing a great opportunity to work with a global company and contribute to their mission.

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