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Clinical Trials Specialist
1 month ago
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.
- 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.
- 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.