Senior Legal Counsel CDDFTC 6 months

il y a 6 heures


Paris, France Owkin Temps plein

Owkin is an AI company on a mission to solve the complexity of biology. It is building the first Biology Super Intelligence (BASI) by combining powerful biological large language models, multimodal patient data and agentic software. At the heart of this system is Owkin K an AI copilot and its new LLM fine‑tuned on biology called Owkin Zero, used by researchers, clinicians and drug developers to better understand biology, validate scientific hypotheses and deliver better diagnostics and therapies faster. The position is based in our Paris offices. Please submit your CV in English. About the role: We are seeking a Senior Legal Counsel to join our Legal team on a fixed‑term basis to cover maternity leave. The role will support the Company’s fast‑growing activities in artificial intelligence applied to healthcare diagnostics and biomedical research with a strong international dimension (primarily Europe and the United States). The Senior Legal Counsel will act as a trusted business partner, providing pragmatic, high‑quality legal support across commercial, R&D, clinical and strategic projects. In particular you will be responsible for: Drafting, reviewing and negotiating licence and services agreements related to the Company’s new AI‑based product for pharmaceutical and biotechnology clients. Drafting and negotiating term sheets and in‑licensing agreements for innovative biotech products. Drafting and negotiating all agreements associated with healthcare research activities and the conduct of clinical trials, including CDMO/CRO supplier and provider agreements, clinical trial agreements (CTAs) and material transfer agreements (MTAs). Drafting and negotiating contracts related to the Group’s diagnostics activities, including commercial licence agreements, distribution agreements and consulting agreements (non‑healthcare professionals) across relevant geographies (mainly Europe and the United States). Providing legal support to the PortrAIt project (consortium), including negotiating specific agreements such as data transfer agreements (DTAs), licence agreements and data processing agreements. Providing day‑to‑day legal support to various departments involved in the Company’s commercial activities and in its healthcare and biomedical product activities, with a particular focus on support related to the conduct of clinical trials and regulatory processes (including CODECOH‑related procedures). Monitoring and providing a legal watch on applicable legislation and regulations in the field of healthcare products, including pharmaceuticals, medical devices and AI‑enabled health technologies. Required Qualifications and Experience: Approximately 8–10 years of professional experience as a lawyer in the life sciences, biotech, pharmaceutical, medical device or digital health sectors. Master’s degree in Health Law (or equivalent) with a specialization in healthcare products strongly preferred. Strong experience in drafting and negotiating complex intellectual property, commercial, R&D and clinical trial‑related agreements. Solid knowledge of applicable regulations relating to healthcare products, including drug development and medical devices in both Europe and the United States. Experience in clinical development, technology transfer, valuation or in‑licensing activities is considered a strong asset. Ability to operate in a fast‑paced, innovative and international environment. Excellent written and verbal communication skills in English (French a plus). Key Skills and Competencies: Strong analytical and drafting skills with a pragmatic and solution‑oriented mindset. Ability to manage multiple matters simultaneously and prioritise effectively. Excellent stakeholder management and business‑partnering capabilities. High level of autonomy, rigor and reliability. Strong ethics and attention to compliance requirements. Collaborative mindset and ability to work cross‑functionally. What we offer: Friendly and informal working environment. Opportunity to work with an international team with high technical and scientific backgrounds. Recruitment Process Please complete the form and submit your CV> Owkin is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, sex, gender, sexual orientation, age, colour, religion, national origin, protected veteran status or on the basis of disability. #J-18808-Ljbffr


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