Clinical Data Lead: EDC & Trial Quality

Meet Life Sciences; Illinois; On-site; USD 90,000 - 120,000; Full time

Job summary

Meet Life Sciences is seeking a Clinical Data Management Specialist to support planning, implementation, and execution of clinical data management across multiple studies. The role leads EDC database development, data review, and cross-functional collaboration throughout the trial lifecycle.

The candidate will design, build, and maintain study databases within an EDC system, configure eCRFs and edit checks, coordinate UAT, and ensure data quality and regulatory compliance.

Qualifications

• Bachelor's degree in Life Sciences or related field.
• 2+ years in Clinical Data Management for clinical trials.
• Hands-on experience designing and programming studies in an EDC system.
• Experience building eCRFs, edit checks, and database validation rules.
• Strong understanding of GCP and data management best practices.
• Experience performing data review, query management, and data cleaning.

Responsibilities

• Lead data management activities from startup through database lock and delivery.
• Develop and maintain study data management documentation (DMPs, edit checks, specs).
• Ensure data accuracy, completeness, and regulatory compliance.
• Participate in study planning and provide data management input during execution.
• Design, build, and maintain EDC study databases and eCRFs.
• Configure data validation rules and UAT for study launches.
• Coordinate database updates, maintenance, and archival tasks.
• Perform ongoing data review, identify missing or erroneous data, and resolve queries.
• Generate data metrics and status updates for stakeholders.
• Collaborate with Cross-Functional teams and external vendors; provide training on EDC.

Skills

Clinical Data Management

EDC design & programming

GCP knowledge

Data quality assurance

Query management

Education

Bachelor's degree in Life Sciences

Job description

Meet Life Sciences is seeking a Clinical Data Management Specialist to support planning, implementation, and execution of clinical data management across multiple studies. The role leads EDC database development, data review, and cross-functional collaboration throughout the trial lifecycle.

The candidate will design, build, and maintain study databases within an EDC system, configure eCRFs and edit checks, coordinate UAT, and ensure data quality and regulatory compliance.