Clinical Data Manager

i-Pharm Consulting; À distance; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A global life sciences organization is seeking a Clinical Data Manager to lead end-to-end data management activities. This fully remote role requires at least 5 years of Clinical Data Management experience within a pharma setting and 3 years of managing global studies. Key responsibilities include ensuring compliance with GCP and regulatory guidelines while mentoring junior team members. The position offers competitive compensation and the chance to work on important client projects in a collaborative environment.

Prestations

Competitive hourly rate

Fully remote role with occasional travel

Collaborative, inclusive culture

Qualifications

• Minimum 5 years’ experience in Clinical Data Management within a pharma setting or CRO.
• At least 3 years’ independent lead experience managing global studies.
• Strong knowledge of GCP, CDISC standards, and clinical trial processes.

Responsabilités

• Manage end-to-end delivery of data management services for projects.
• Act as the primary point of contact for client data management deliverables.
• Ensure compliance with GCP, SOPs, and regulatory guidelines.

Connaissances

Clinical Data Management

Project Management

Communication

Stakeholder Engagement

Description du poste

Clinical Data Manager – France

Contract | Full-time | Remote

Are you an experienced Clinical Data Manager with a proven track record of leading end-to-end data management activities?

We are seeking a Data Management professional to join a dedicated team supporting a critical client project within a global life sciences organisation.

This role offers the opportunity to work across the full data management lifecycle, ensuring high-quality deliverables, compliance with regulatory standards, and strong client engagement.

Key Responsibilities

• Manage end-to-end delivery of data management services for single/multi-service projects.
• Act as the primary point of contact for client data management deliverables.
• Lead project planning, execution, and close-out, including financial tracking and invoicing.
• Ensure compliance with GCP, SOPs, and regulatory guidelines.
• Mentor and train junior Data Managers, providing subject matter expertise.
• Drive process improvements and implement new technologies/tools.
• Maintain audit‑ready documentation and ensure timely database lock.

Skills & Experience

• Minimum 5 years’ experience in Clinical Data Management within a pharma setting or CRO.
• At least 3 years’ independent lead experience managing global studies.
• Strong knowledge of GCP, CDISC standards, and clinical trial processes.
• Excellent project management, communication, and stakeholder engagement skills.
• Ability to manage financial aspects (budget tracking, revenue recognition).

What’s on Offer

• Competitive hourly rate.
• Fully remote role with occasional travel (up to 25%).
• Opportunity to work on a critical client project within a global organisation.
• Exposure to diverse therapeutic areas and innovative clinical programs.
• Collaborative, inclusive culture where your expertise makes a real impact.

If you are a proactive leader with deep expertise in clinical data management and a passion for delivering quality outcomes, we’d love to hear from you.

Apply now to take the next step in your career!