OKILYS Life Science is a France-based EURL (freelance consultancy) specialized in clinical trial operations and regulatory affairs, supporting CROs, sponsors, and academic institutions in France and Belgium.

With over 11 years of experience in clinical research, including 5+ years as a freelance consultant, I offer flexible and reliable support across key functional areas:

✅ Regulatory & Ethics Submissions (ANSM, CPP, AFMPS, CTIS, CNIL, CNOM, ARS)
✅ Site Start-Up & Activation (France & Belgium – EU-CTR, RIPH/RNIPH)
✅ Contract & Budget Negotiation (Convention Unique, Direct Contracts, Pharma.be)
✅ Monitoring & Site Oversight (Phases I to IV – on-site & remote)
✅ Team coordination, communication & training

Thanks to a cross-functional and adaptable profile, I can seamlessly support roles such as:
🔹 SSU Specialist
🔹 Contract & Budget Manager
🔹 Senior CRA
🔹 Clinical Trial Lead / Project Manager
🔹 Line Manager (CRA/SSU)

📍 Based in Bourgogne-Franche-Comté – Operating remotely across Europe
🌐 Services available in French and English

Let’s collaborate to move your trials forward — on time, with quality and compliance.

📩 lydie.parsus@okilys.com
🔗 www.linkedin.com/in/lydie-parsus (if you wish to add)

OKILYS Life Science

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OKILYS Life Science

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