Clinical Research Data Manager

By | February 12, 2025

Clinical Research Data Manager

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Job ID: 9728026

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Remote, WI, US

Scientific

Bachelors Degree

Full Time, Temporary

Experienced (Non-Manager)

Remote

Healthcare Services

First Shift (Day)

Remote, WI, US

Experienced (Non-Manager)

Full Time, Temporary

Healthcare Services

Remote

Scientific

Bachelors Degree

First Shift (Day)

Apply Now Applied

Job details

Clinical Research Data Manager (100% Remote, 12-Month Contract)

Are you an experienced Clinical Research Data Manager looking for an exciting opportunity to support cutting-edge medical device clinical trials? Join our team and play a critical role in ensuring high-quality, regulatory-compliant data management that drives medical innovation.

Why You’ll Love This Role:

? 100% Remote – Work from anywhere
? Contribute to life-changing medical research
? Collaborate with top-tier Clinical Operations and Research teams
? Competitive 12-month contract with the potential for extension

What You’ll Do:

  • Lead data management activities for multiple clinical trials, ensuring compliance with Good Clinical Practices (GCP) and ISO 14155.

  • Develop and maintain study-specific documents (DMPs, DVPs, CCGs, CRFs) and build clinical trial databases.

  • Partner with Clinical Operations, Study Monitors, and Statisticians to optimize data strategy and execution.

  • Utilize Electronic Data Capture (EDC) platforms, including Veeva CDMS or RedCap, to build and validate databases.

  • Design Custom Functions using C# and develop dashboards with Power BI, Tableau, or similar tools.

  • Ensure data integrity, regulatory compliance, and efficiency in clinical trials.

What You Bring:

? Bachelor’s degree (Computer Science, Healthcare, or related field) OR 6+ years of clinical data management experience in Pharmaceuticals/Biotech/Medical Devices.
? Hands-on experience with EDC systems, including database building, validation, and decommissioning.
? Strong knowledge of clinical research operations, regulatory requirements, and data privacy laws.
? Technical proficiency in database management, programming languages (C#, Java, XML), and clinical data tools.
? Ability to manage multiple projects, drive collaboration, and implement process improvements.

Preferred Skills (Nice to Have):

  • Experience with Veeva CDMS, RedCap, or Business Intelligence tools (Power BI, Spotfire, Tableau).

  • Familiarity with Quality Management Systems (QMS), GDP, and CAPA processes.

  • Strong problem-solving and project management abilities.

? Be a part of something bigger—help shape the future of medical research!

? Ready to apply? Submit your resume today!

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