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# Analyst, Clinical Data Mgmt

- **Company:** Spectraforce
- **Location:** Irvine, CA, United States
- **Experience:** Experienced
- **Contract:** Temporary contract
- **Skills:** Clinical Data Management, Clinical Data Repository, Databases, Coherent Remote File System (CRFS), Electronic Data Capture, Microsoft Office, Software Tools, Clinical Data Management System, Test Scripts, Data Management
- **Published:** September 9, 2026
- **Apply:** http://leoforce.us/Careers/Spectraforce/JobDetails.html?jobid=dad370e2-ed44-4852-a219-1da2e2c70e63&OrgId=1&UserId=1173

## About the Role

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

## Description

* The main function of a clinical data analyst is to lead and support clinical data management activities, during study start-up, conduct and closeout, including database lock., * 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.


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