Clinical Contract Manager

Ipsen; Paris; Sur place; EUR 70 000 - 110 000; Plein temps

Résumé du poste

Ipsen, a patient-focused biopharmaceutical company based in Paris, seeks a Clinical Contract Manager to ensure contracts and data privacy across clinical studies comply with legal and regulatory standards.

You will support Global Medical Clinical Operations, oversee the CCA team, and guide study start-up and execution with pragmatic, compliant solutions. Fluency in English is required; French is a plus.

Qualifications

• Master's degree in Law is mandatory.
• Proven experience in clinical contract negotiation and/or data privacy compliance.

Responsabilités

• Provide expert oversight on clinical contracts and data privacy topics.
• Advise Clinical Operations teams to facilitate study start-up and execution with compliance in mind.
• Co-lead recruitment and onboarding for the Clinical Contract Associate team.
• Define onboarding and training programs for contracting processes and SOPs.

Connaissances

Contract negotiation

Data privacy

Regulatory compliance

Advisory & training

Cross-functional collaboration

Formation

Master's degree in Law

Description du poste

Are you ready to lead and innovate in a dynamic, patient-focused biopharmaceutical company?

Ipsen is a growing global specialty-driven biopharmaceutical company focused on innovation and specialty care. We aim to make a sustainable difference by significantly improving patients’ health and quality of life, providing effective therapeutic solutions for unmet medical needs through differentiated and innovative medicines in Oncology, Neurosciences, and Rare Diseases.

Why Ipsen?

Patient-Focused: The patient is at the heart of everything we do, and improving their outcomes is the deliverable of every strategy.

Employee Care: We care for our employees, who are the ambassadors making a real difference.

Bold Leadership: We attract and develop bold, agile, entrepreneurial individuals who take full ownership of their decisions.

Growth Opportunities: We offer a wealth of fulfilling challenges and growth opportunities in a fast-moving, game-changing organization.

About The Role

The Clinical Contract Manager ensures that clinical research activities are conducted in full compliance with applicable legal, regulatory, contractual, and data privacy requirements, and oversees the Clinical Contract Associate (CCA) team activities.

Positioned within Global Medical Clinical Operations / Clinical Excellence, you provide expert support and oversight on contracts managed by the department (clinical studies, managed access programs, contractors) and data protection matters, enabling compliant and efficient study execution while safeguarding patient data and Ipsen’s legal obligations.

Main Responsibilities

Clinical Contracts Compliance

Applicable to studies and programs managed by Global Medical Clinical Operations or any potential other activities delegated by global legal

• Provide expert oversight and guidance on agreements,
• Ensure contractual content is fully compliant with applicable legal, regulatory, and data protection requirements.

Data Privacy & GDPR Compliance

• Act as the clinical data privacy champion for Global Medical Clinical Operations.
• Ensure compliance with GDPR and/or any applicable data protection laws for clinical studies, registries and Managed Access Programs.
• Review and support privacy‑related documentation

Advisory, Training & Operational Support

• Act as a trusted advisor to Clinical Operations teams on clinical contracts and data privacy topics.
• Provide pragmatic, solution‑oriented guidance to facilitate study start‑up and execution while maintaining legal compliance.

Clinical Contract Associate (CCA) Team oversight

• Co-lead with the head of function, the recruitment process for the CCA team (workforce planning, job descriptions, interviews, selection, and onboarding).
• Define, deploy, and continuously improve the onboarding and training program to ensure consistent understanding of clinical contracting processes, compliance requirements, and internal SOPs.

Qualifications

• Master's degree in Law (mandatory)
• Proven experience in clinical contract negotiation and/or data privacy compliance within the pharmaceutical, biotechnology, or CRO industry
• Prior experience working within the pharmaceutical industry.
• Strong working knowledge of GDPR, data protection regulations in clinical research, and clinical contracting frameworks
• Solid expertise in data protection and data privacy
• Fluent in English (written and spoken)
• French is a plus