Senior Clinical Data Management Leader

Integra LifeSciences; Princeton (NJ); Hybrid; USD 109,250 - 149,500; Full time

Benefits offered by this job

Medical, dental, vision

Life insurance

Disability

401(k)

Job summary

Integra LifeSciences in Princeton, NJ, is seeking a Senior Clinical Data Manager to lead end-to-end data management for multiple studies, providing strategic input into study planning, execution, and risk mitigation.

You will ensure GCP compliance, oversee vendor performance, mentor data management staff, and collaborate with Biostatistics, Medical Affairs and study teams to deliver high-quality data outputs on time.

Qualifications

• Bachelor’s degree in life sciences, data science or related field.
• CCD M certification is a plus.
• Minimum of 10 years of progressive experience in clinical data management within pharma/biotech/medical device/CRO environments.

Responsibilities

• Lead and oversee end-to-end clinical data management activities across assigned studies and projects.
• Provide strategic input into study planning, execution, and risk mitigation.
• Drive continuous improvement initiatives, contributing to GSOPs and data management strategy.
• Provide strategic input in database design and data review/ cleaning, query management and database lock activities.
• Ensure compliance with GCP, GSOPs and regulatory requirements.
• Oversee vendor performance and act as escalation point for quality, timeline and scope issues.
• Represent data management in cross-functional forums to ensure data deliverables are high quality and timely.
• Mentor and onboard data management staff to build team capabilities.

Skills

Leadership

EDC systems

Stakeholder management

Prioritization

Problem solving

Vendor management

Education

Bachelor’s degree in life sciences, data science or related field

CCDM certification (or equivalent)

Tools

Veeva CDMS

Veeva eTMF

Job description

Integra LifeSciences in Princeton, NJ, is seeking a Senior Clinical Data Manager to lead end-to-end data management for multiple studies, providing strategic input into study planning, execution, and risk mitigation.

You will ensure GCP compliance, oversee vendor performance, mentor data management staff, and collaborate with Biostatistics, Medical Affairs and study teams to deliver high-quality data outputs on time.