Responsible for overseeing the end-to-end contract documentation process, ensuring quality control throughout. This includes managing the execution of contracts and amendments, and distributing them to relevant third parties as needed. Duties also involve data entry, generating reports from tracking databases, following up with third parties regarding contract and amendment execution, and maintaining up-to-date on-site paper files.
This is a hybrid role, requiring two days per week on-site at the client’s office in Paris.
We are looking for a Clinical Trial Assistant (CTA) or Clinical Trial Coordinator (CTC) with prior experience in the pharmaceutical or CRO industry. The ideal candidate will have a background in Finance or Legal, preferably with previous exposure to Payments or Pricing. This role will support contract management and the preparation of economic reports, so a strong eye for detail and experience working with financial or contractual documentation is essential.
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