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TechData Service Company LLC

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Clinical Data Management Analyst (19151-1)

Irvine, CA · On-site

$38 - $48/hr

Job ID: 19151-1 Job Title: Clinical Data Management Analyst Job Length: 1 Year (Renewable) Compensation: Up to Summary: Up to $48/hr. Location: Irvine, CA 92606 Key Responsibilities: * Define and ...

TJX Companies

Admin Coordinator

Philadelphia, PA · On-site

$13 - $13.50/hr

TJ Maxx Store 0736 || 7616 City Line Ave || Philadelphia || PA || 19151 Opportunity: Contribute To The Growth Of Your Career Supports store management in the execution of store related administrative ...

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What does a typical workday look like for an Air Force Aircrew Egress Systems Specialist?

As an Aircrew Egress Systems Specialist, your daily duties include inspecting, maintaining, and repairing aircraft ejection seats, canopies, and life support systems to ensure aircrew safety. You'll often work within a maintenance squadron, collaborating with other specialists to address scheduled and emergency repair needs. The role involves detailed technical documentation, system testing, and strict adherence to safety standards. This position offers a mix of hands-on mechanical tasks and teamwork within a highly structured, safety-focused environment, with numerous opportunities for advanced technical training and leadership roles.

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Infographic showing various 19151 job openings in the United States as of July 2026, with employment types broken down into 43% Full Time, and 57% Part Time. Highlights an 100% Physical job distribution.

Clinical Data Management Analyst (19151-1)

Irvine, CA • On-site

TechData Service Company LLC
Biotechnology Research and Development • 51 - 200 employees
Learn more about TechData Service Company LLCexternal

$38 - $48/hr

Contractor

Medical, Dental, Vision

Posted 6 days ago

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Job description

Job description:

Job ID: 19151-1
Job Title: Clinical Data Management Analyst
Job Length: 1 Year (Renewable)
Compensation: Up to
Summary: Up to $48/hr.
Location: Irvine, CA 92606




Key Responsibilities:

  • Define and specify clinically data collection requirements (e.g., eCRFs, CRFs, edit checks and collection of external data) for assigned studies; including defining, performing, using Global Library standards and coordinating user acceptance testing (e.g. test scripts and checklists) to ensure appropriate data are collected.
  • Evaluate data errors and collection issues; provide guidance and recommendations to clinical team for resolution.
  • Lead project management activities for clinical studies on-line, including conducting project team meetings, establishing and maintaining project timelines, and communications to stakeholders.
  • Maintain and develop Data Management deliverables including data management plans (DMPs), training materials and user aids in compliance with regulations.
  • Perform User Access and data (external and internal) reconciliation.
  • Experience with Trial Master File (TMF) for clinical trial documentation and filing.
  • Participate in review of SOPs, work instructions, and associated documents for CDM, including recommending revisions and updates to SOPs, participating in the development of user training.

Skills:

  • Experience with EDC (Electronic Data Capture) systems required, both Classic and New Medidata RAVE EDC.
  • Good computer skills in Microsoft Office Suite.
  • Good written and verbal communication skills and interpersonal relationship skills.
  • Good problem-solving and critical thinking skills.
  • Experience with using AI tools like CoPilot, Claude to support clinical trial activities is preferred.

Education and Experience:

  • Bachelor's Degree or equivalent.
  • 2-4 years of experience required.

Benefits:


  • Dental insurance
  • Health insurance
  • Vision insurance


Work Location: In person

Company Description

https://quantive.bio/