Full-Time Site Administrator
PSI CRO is hiring a remote Full-Time Site Administrator. The career level for this job opening is Entry Level and is accepting Remote based applicants remotely. Read complete job description before applying.
PSI CRO
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- Assist with the coordination and execution of clinical research studies.
- Screen and recruit study participants.
- Assist with data entry of clinical trial information.
- Assist in scheduling participant visits and follow-ups.
- Maintain study documentation, including staff credentials and regulatory files.
- Maintain files for SOP’s and other internal files as delegated.
- Ensure all study activities follow Good Clinical Practice (GCP) guidelines and IRB requirements.
- Prepare and organize study materials, equipment, and supplies.
- Support the research team in compiling reports and preparing data for analysis.
- Attend study meetings and training sessions as required.
The Site Administrator reports to the Milestone One Manager. The scope of the Site Administrator’s responsibilities will be clearly defined for each project.
Education: High school degree or equivalent. Current Good Clinical Practice (GCP) may be obtained during orientation.
Experience: Experienced in a clinical research setting for at least 1 year. Must demonstrate clinical research and general medical terminology proficiency. Must have experience with initial IRB submission and maintenance requirements and procedures.
Skills: Strong organizational and time-management skills. Attention to detail. Proficiency in MS Office.
Behavioral Skills: Excellent communications skills. Effective problem-solving and result-oriented. Accountability. Team player.