Clinical Data Manager

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

Résumé du poste

A leading global life sciences consultancy seeks a Clinical Data Manager to oversee end-to-end data management for critical client projects. The ideal candidate will bring over 5 years of experience in Clinical Data Management, with independent leadership over global studies. Excellent knowledge of GCP and CDISC standards is essential. This fully remote role includes occasional travel, promoting a collaborative culture where expertise impacts diverse therapeutic areas.

Prestations

Competitive hourly rate

Fully remote role

Opportunity for occasional travel

Qualifications

• 5+ years experience in Clinical Data Management in pharma or CRO.
• At least 3 years leading global studies independently.
• Strong understanding of GCP and clinical trial processes.

Responsabilités

• Manage end-to-end delivery of data management services.
• Act as primary contact for client data management deliverables.
• Lead project planning, execution, and close-out.

Connaissances

Clinical Data Management

GCP

CDISC standards

Project management

Communication skills

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!