Senior Clinical Data Manager — Remote/Hybrid Lead

Allucent; Paris; Hybrid; EUR 80,000 - 110,000; Full time

Benefits offered by this job

Benefits per location

Flexible hours

Career progression

Buddy program

Training budget

Job summary

Allucent is seeking a Sr. Clinical Data Manager to lead data management for clinical trials in a hybrid/remote setting. You will oversee DM deliverables from study design through database lock, ensuring data integrity, regulatory compliance, and timely study conclusions.

You will collaborate with multi-disciplinary teams, contribute to DM standards, train staff, and drive process improvements to support global biopharmaceutical projects.

Qualifications

• Life science/healthcare degree required or equivalent experience.
• Minimum 5 years as Clinical Data Manager in CRO environment.
• Strong knowledge of ICH-GCP, 21 CFR 11, GDPR/HIPPA.
• Experience with EDC systems (IRT, eCOA) and data management in clinical trials.

Responsibilities

• Lead DM activities from database design to lock, ensuring data quality and regulatory compliance.
• Coordinate cross-functional teams and external partners (sponsors, vendors, sites).
• Develop and maintain DM documents (DMP, eCRF specifications, DVP, data transfers).
• Oversee UAT, data cleaning strategies, and data reconciliation activities.
• Mentor staff and contribute to training and process improvements.

Skills

Project management

Data management

CDISC standards

EDC systems

Regulatory knowledge

English language

Stakeholder management

Documentation

Education

Life science/Healthcare degree

Tools

EDC software

IRT

eCOA

MS Office

Job description

Allucent is seeking a Sr. Clinical Data Manager to lead data management for clinical trials in a hybrid/remote setting. You will oversee DM deliverables from study design through database lock, ensuring data integrity, regulatory compliance, and timely study conclusions.

You will collaborate with multi-disciplinary teams, contribute to DM standards, train staff, and drive process improvements to support global biopharmaceutical projects.