· Review and assess a variety of agreements related to clinical trials, including but not limited to clinical trial agreements, service agreements, consultancy agreements, and confidentiality agreements.

· Provide legal support on non-clinical trial matters, including the development of legal presentations, implementation of IT tools, and addressing intellectual property issues.

· Assist in drafting, reviewing, and negotiating various contracts such as confidentiality agreements, consultancy agreements, service agreements, material transfer agreements, and contract amendments, all under the supervision of a legal advisor.

· Participate actively in internal project meetings, collaborating with internal teams as well as external stakeholders, including third parties and external legal counsel when necessary.

· Handle administrative tasks such as managing document signatures, maintaining an organized filing system, and ensuring efficient use of tracking systems.

· Law degree (Paralegal, Bachelor’s, or equivalent) with 5-7 years of experience in contract negotiation and drafting.

· Fluent in both English and French (C1 level), with excellent written and verbal communication skills.

· Experience in the Life Sciences sector is preferred, with a background in Intellectual Property considered a strong asset.

· Outstanding interpersonal skills, capable of collaborating effectively within an international, multidisciplinary environment.

· Self-driven with the ability to work independently while maintaining a strong team-oriented approach.

· Exceptional organizational skills with the ability to prioritize tasks and manage multiple projects efficiently.