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Clinical Trials Specialist

1 month ago


Horsham, West Sussex, United Kingdom Cmed Group Ltd Full time
Cmed Group Ltd: A Leading CRO

We are seeking a skilled Clinical Trials Specialist to join our team at Cmed Group Ltd, a renowned Contract Research Organization (CRO). The successful candidate will support General Counsel on contract review process for clinical site agreements, NDAs, CDAs, and other commercial agreements.

Key Responsibilities:
  • Review, edit, and draft commercial agreements, including clinical site agreements and NDAs.
  • Collaborate with General Counsel to support contract review process.
Required Skills and Qualifications:
  • Minimum of 2 years hands-on experience reviewing clinical site contracts in a pharma or CRO environment.
  • General commercial contracts experience within a clinical trials environment.
  • Strong appreciation of contract law with a good legal understanding from previous in-house experience in a contracts role.
  • Previous exposure of dealing with sites and investigators located in EU and the USA highly desirable.
  • Excellent communication skills, both written and verbal in English with second European language desirable.
  • Strong attention to detail and proven drafting skills.
Benefits:
  • Opportunity to be part of an innovative organization and work with exciting technologies.
  • Mentorship and training to further develop your skills in the clinical trials industry.
  • Competitive employment package.