Review, draft, negotiate and track a variety of legal agreements including confidentiality disclosure agreements (CDA), initial clinical trial agreements (CTA), amendments to the clinical trial agreements (CTA-A), site budgets and other various types of documents. Will work closely with the Clinical Operations study team and play an administrative role to ensure deliverables are in alignment with defined project timelines and expectations.
Other Required:
- 3 years of relevant experience drafting, reviewing and negotiating agreements related to clinical
research i.e. Non-Disclosure Agreements, Clinical Trial Agreements, etc. as well as management, control and tracking of the contract process.
- Experience in contract research, life science, biotech or pharmaceutical industry is preferred.
- Experience interacting with European institutions.
Preferred:
- Equivalent contract management experience in a clinical research or similar industry setting
- Experience in contract research, life science, biotech or pharmaceutical industry.
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