Regulatory Contract Reviewer
6 days ago
We are seeking a talented Regulatory Contract Reviewer to join our team at Cmed Group Ltd, an International Contract Research Organization (CRO) based in the UK or EU. As a key member of our team, you will play a vital role in supporting our clinical trials operations.
The successful candidate will have a minimum of 2 years' experience reviewing clinical site contracts in a pharma or CRO environment, with a strong focus on commercial contract knowledge and excellent communication skills.
Your key responsibilities will include reviewing, editing, and drafting commercial agreements, including clinical site agreements and NDAs. You will also collaborate with our General Counsel to support contract review processes.
- Key qualifications and attributes:
- 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.
- Available to start immediately or at short notice.
- What we offer:
- Opportunity to work with a dynamic and innovative organization.
- Mentorship and training to further develop your skills in the clinical trials industry.
- Competitive employment package (£40,000 - £60,000 per annum).
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