Senior Clinical Data Manager: Lead CDM Projects

MMS; Raleigh (NC); On-site; USD 90,000 - 130,000; Full time

Job summary

MMS is a data-focused CRO seeking a seasoned Data Manager to lead data management efforts across study lifecycles. You will oversee data handling from setup to close-out and coordinate across clients and suppliers to ensure timely, accurate data delivery.

The role requires deep knowledge of EDC systems, CRFs, and hybrid CDM workflows, plus strong communication and mentoring abilities. Join MMS to contribute to high-quality regulatory submissions and innovative trial data solutions.

Qualifications

• 5+ years in data management with at least 1 year leading projects.
• Extensive knowledge of paper CRFs, EDC, and hybrid CDM systems.
• Strong knowledge of Clinical Operations SOPs and working practices.

Responsibilities

• Oversee data management from study setup to close-out; primary DM contact.
• Coordinate data management activities and timelines across cross-functional teams.
• Maintain data quality through validation, edits, and data reconciliation.
• Train and mentor junior data managers; support QA/QC activities.
• Ensure compliance with GCP/ICH guidelines and FDA regulations as applicable.

Skills

Data management

Project leadership

Communication

EDC systems knowledge

Education

Bachelor’s or Master’s Degree in scientific or health care field

Tools

EDC systems

Clinical data management tools

Job description

MMS is a data-focused CRO seeking a seasoned Data Manager to lead data management efforts across study lifecycles. You will oversee data handling from setup to close-out and coordinate across clients and suppliers to ensure timely, accurate data delivery.

The role requires deep knowledge of EDC systems, CRFs, and hybrid CDM workflows, plus strong communication and mentoring abilities. Join MMS to contribute to high-quality regulatory submissions and innovative trial data solutions.