Clinical Project Manager

JR France; Limoges; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading company in the field of Haematology Gene Therapy is looking for an experienced Freelance Clinical Project Manager. The role involves overseeing clinical trial execution, managing regulatory submissions, and ensuring compliance with EU regulations. The ideal candidate will have a strong background in project management and leadership, along with fluency in English. This position offers the opportunity to work closely with various stakeholders to ensure the success of clinical studies.

Qualifications

• Minimum 5 years of clinical trial project management experience.
• Experience in Haematology Gene Therapy is a strong advantage.

Responsabilités

• Oversee all aspects of clinical trial execution.
• Manage regulatory submissions and ethics committee documentation.
• Monitor site activation, patient recruitment, and ongoing study progress.

Connaissances

Leadership

Communication

Problem Solving

Fluency in English

Description du poste

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Freelance CPM - France- Haematology Gene-Therapy

Upsilon Global is seeking an experienced Freelance Clinical Project Manager to oversee a Haematology Gene Therapy study in France.

● Therapeutic Area: Hematology Gene Therapy

Key Responsibilities:

● Oversee all aspects of clinical trial execution, ensuring adherence to timelines, budgets, and quality standards.

● Manage regulatory submissions and ethics committee documentation in line with French and EU requirements.

● Monitor site activation, patient recruitment, and ongoing study progress, proactively addressing challenges.

● Collaborate closely with sponsors, investigators, vendors, and regulatory authorities to ensure smooth study operations.

● Identify study risks and implement effective mitigation strategies throughout the project lifecycle.

● Provide leadership and guidance to clinical research teams, supporting training and performance.

● Ensure compliance with ICH-GCP, local regulations, and gene therapy-specific guidelines.

Requirements:

● Minimum 5 years of clinical trial project management experience.

● Experience in Haematology Gene Therapy is a strong advantage.

● In-depth knowledge of EU clinical trial regulations and GCP guidelines.

● Strong leadership, communication, and problem-solving skills.

● Fluency in English required; French is a plus.

For more details please contact Amani Manaka or call [phone]