Research Assistant III, Lab at Dynamed Clinical Research
Overview
Owns data collection and regulatory support for clinical trials at a hospital-based site. Scale includes coordination of samples, study documentation, and site visits across multiple protocols. Works with the clinical research team and monitors to ensure compliance and data integrity. This role differs by combining hands-on patient interactions with regulatory documentation and data capture in EDC systems.
What You'll Do10
- 1Build source documents and regulatory binders for assigned protocols
- 2Design and maintain accurate patient data in the EDC/IVRS systems
- 3Lead shipment and tracking of subjects samples per Sponsor requirements
- 4Ship and manage specimens per protocol and guidance documents
- 5Drive preparation for monitoring visits and audits by ensuring up-to-date protocols and ICFs are used
- 6Assist in reporting Adverse Events per sponsor requirements
- 7Coordinate with investigators and staff to address monitoring findings
- 8Maintain detailed records and prepare for study-related meetings
- 9Assist in compilation of regulatory documentation for site audits
- 10Contribute to study data quality and compliance during patient visits
Requirements8
- 1High school diploma or equivalent required
- 2Prior clinical research experience preferred
- 3Phlebotomist certificate preferred
- 4Medical Assistant Certification preferred
- 5Knowledge of medical terminology required
- 6Detail-oriented and able to maintain accurate records
- 7Excellent customer service and computer skills
- 8Availability for site visits and monitoring as required
Salary Insight
Salary not disclosed in listing
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