Philadelphia, Pennsylvania, United States of America
Good clinical research practice (gcp)
Protocol coordination
Biological specimen management
Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP)
Job Summary
Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP).
Prepares and submits all materials for the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol to ensure compliance in a timely fashion.
Jefferson offers a comprehensive package of benefits for full-time and part-time colleagues, including medical, dental, vision, and retirement plans.
Matching Summary
Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP).
Skills & Requirements
Must-have
Good Clinical Research Practice (GCP)
protocol coordination
biological specimen management
regulatory and/or IRB document preparation
quality control assessments
Nice-to-have
orientation and training of new staff
development of workflows
SOP/guidance document revision
participates in work groups
Key Requirements
High School Diploma/GED and 5 years experience
SoCRA certification
6 years clinical research experience
2 years with Bachelor's degree and 2 years experience