Clinical Data Coordinator
GForce Life SciencesSanta Clarita, CA, United Statesjob_description.job_card.variable_hours_ago
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job_description.job_card.job_descriptionBachelor’s degree in a scientific or health-related field preferred. 1–3 years of experience in clinical data management or related area. Proficiency with Microsoft Office applications (Excel, Word, Outlook). Strong organizational skills, attention to detail, and communication abilities. Familiarity with EDC systems and Good Clinical Data Management Practices is a plus.
Clinical Data Coordinator
6 month contract
Must be able to work on a W2
100% on-site in Sylmar, CA - 7 AM - 3 : 30 PM (Flexible)
We are seeking a Clinical Data Coordinator to support both electronic and paper-based clinical studies. In this role, you will ensure the accuracy and integrity of clinical data across multiple studies and maintain compliance with Good Clinical Data Management Practices. This position requires strong attention to detail, organizational skills, and the ability to collaborate effectively within a global clinical team.
Job Responsibilities :
- Perform data entry, data cleaning, and updates in accordance with study protocols and approved guidelines.
- Review and process Data Clarification Forms and ensure timely resolution of data discrepancies.
- Maintain and file processed clinical documents to support data integrity and traceability.
- Support the setup and maintenance of EDC systems and paper-based studies.
- Ensure compliance with Good Clinical Data Management Practices (GCDMP).
- Collaborate with internal and external study teams to maintain data quality and consistency.
Qualifications :
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Clinical Coordinator • Santa Clarita, CA, United States