Clinical Project Manager

JR France; Aix-en-Provence; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading company in France is seeking an experienced Freelance Clinical Project Manager for a Hematology Gene Therapy study. The role involves overseeing clinical trial execution, managing regulatory submissions, and collaborating with various stakeholders. Ideal candidates will have a strong background in clinical project management, particularly in Hematology Gene Therapy, and possess excellent leadership and communication skills.

Qualifications

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

Responsabilités

• Oversee all aspects of clinical trial execution.
• Manage regulatory submissions and ethics committee documentation.
• Collaborate closely with sponsors and investigators.

Connaissances

Leadership

Communication

Problem-Solving

Fluency in English

Description du poste

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Clinical Project Manager, Aix-en-Provence

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Client:

Location:

Aix-en-Provence, France

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

382054920280342528327611

Job Views:

2

Posted:

15.05.2025

Expiry Date:

29.06.2025

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Job Description:

Freelance CPM - France - Hematology Gene Therapy

Upsilon Global is seeking an experienced Freelance Clinical Project Manager to oversee a Hematology 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 Hematology 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].