Title: CRA/Sr CRA & Global Technical Advisor
Company: Precision Healthcare
Location: Remote/Onsite (25%)
The CDC’s Division of Global HIV & Tuberculosis (DGHT) is a partner in the unified U.S. Government effort to implement the President’s Emergency Plan for AIDS Relief (PEPFAR). The CDC DGHT team assists resource strained countries address the global HIV/AIDS pandemic by preventing infection, improving treatment, care, and building infrastructure and capacity that support populations living with HIV.
Precision supports the CDC’s mission by providing qualified clinicians to monitor the progress oversight of protocol-directed research in Africa and Asia. We currently seek the following:
-PT (Per Diem) Clinical Research Associates (CRA)
-FT Senior Clinical Research Associates (Sr CRA)
-PT (Per Diem) Global Technical Advisor
CRA/Sr CRA Duties:
CRAs manage the internal and external monitoring of protocol-directed activities to ensure the rights and well-being of study participants are protected. This includes informed consent, validating that research data is complete from verifiable source documents and complies with current IRB approved Protocols, SOPs, GCP, GLP (if applicable), and other regulatory requirements.
Requirements: B.S. degree and/or M.S.,M.A. degree in Public Health/related field; CRA certification (ACRP, CCRA, SOCRA) preferred; 5+ years U.S. clinical research experience and infectious disease monitoring. International monitoring is a plus; Familiar with IRB Policies/Reporting, CRF data verification, IC, GCP, and corrective and preventive action plan development.
Global Technical Advisor:
This role supports the project as a Subject Matter Expert for HIV/TB Research, Monitoring and Evaluation. Providing assistance in technical and operational research strategy for HIV/TB. Develops and reviews monitoring tool resources and provides capacity building assistance, clinical analytics, and project evaluation.
Requirements: B.S. degree and/or M.S.,M.A. degree Public Health/related field; CRA certification (ACRP, CCRA, SOCRA) preferred;
8+ years U.S. clinical research experience and infectious disease
monitoring; International monitoring a plus; Understands IRB Policy/Reporting, CRF data verification, IC, corrective and preventive action plan development, and GCP training experience.
To apply for this position or to learn more, please contact firstname.lastname@example.org.
SOCRA Exp: 12/28/2022