Senior Clinical Data Manager: Data Quality & DM Oversight

Katalyst CRO; Omaha (NE); On-site; USD 80,000 - 100,000; Full time

Job summary

A leading clinical research organization in Omaha is seeking a Mid-Senior level Data Management Lead. In this contract role, you will oversee all data management activities from database startup to lock, ensure compliance with all DM-related documents, and interact with various stakeholders including internal teams and third-party vendors to maintain data quality. Ideal candidates have 8+ years of relevant experience and a strong IT or scientific background, with familiarity in EDC software and regulatory requirements.

Qualifications

• 8+ years of data management experience in a pharmaceutical, biotech or CRO setting.
• Familiarity with CDISC/CDASH and standard international coding dictionaries.
• Experience in managing Trial Master files and various EDC software.

Responsibilities

• Oversee all data management CRO activities from start-up to database lock.
• Work with DM CROs to develop study timelines and ensure deliverables.
• Responsible for review of study-related metrics, reports, and logs.

Skills

Data management experience

Clinical research experience

Project management skills

Strong organizational skills

Effective communication skills

Education

Bachelor's degree in a science-related field or IT

Tools

Medidata RAVE

Oracle

Microsoft Office Suite

Job description

A leading clinical research organization in Omaha is seeking a Mid-Senior level Data Management Lead. In this contract role, you will oversee all data management activities from database startup to lock, ensure compliance with all DM-related documents, and interact with various stakeholders including internal teams and third-party vendors to maintain data quality. Ideal candidates have 8+ years of relevant experience and a strong IT or scientific background, with familiarity in EDC software and regulatory requirements.