Senior Clinical Data Manager - Medical Device Trials

Regulatory Jobs; Kennesaw (GA); On-site; USD 120,000 - 160,000; Full time

Job summary

Artivion, Inc. is seeking a Sr. Clinical Data Manager responsible for data management operations across studies and projects.

This role covers database setup, study documentation, training, data review, query resolution, and database maintenance to ensure data integrity from start-up to lock. It also includes data support for department projects and inquiries unrelated to studies. The position requires leading end-to-end data management activities, development of DMPs and CRFs, overseeing

Qualifications

• Requires Bachelor's or Master’s degree in Life Sciences, Data Science, Computer Science, or related field.
• 7+ years of clinical data management experience, with at least 2 years in a senior or lead role.

Responsibilities

• Lead end-to-end data management activities for clinical trials (inhouse or CROs).
• Develop and maintain Data Management Plans (DMPs), CRFs, edit check specs, and other docs.
• Oversee database build and testing including UAT in EDC systems.
• Ensure data integrity, timely data collection, cleaning, reconciliation, and database lock.
• Collaborate with Clinical Operations, Biostatistics, Regulatory Affairs, QA, and CROs/vendors.

Skills

Leadership

Communication

Data management

Education

Bachelor's degree in Life Sciences

Master’s degree in Life Sciences

Tools

EDC systems

CDISC (CDASH/SDTM)

Job description

Artivion, Inc. is seeking a Sr. Clinical Data Manager responsible for data management operations across studies and projects.

This role covers database setup, study documentation, training, data review, query resolution, and database maintenance to ensure data integrity from start-up to lock. It also includes data support for department projects and inquiries unrelated to studies. The position requires leading end-to-end data management activities, development of DMPs and CRFs, overseeing