Job Description
Job Overview
Work as an integral member of investigator site staff managing the day-to-day coordination and execution of clinical studies in accordance with the protocol, contracted scope of work, good clinical practice, sponsor and standard operating procedures (SOPs) and any relevant local guidelines and regulations.
Essential Functions
• Provide clinical research support to investigators to prepare for and execute assigned research studies
• Review study protocols, source document forms, other study-specific documents, and electronic data capture systems used to record clinical research data
• Collect and submit regulatory/ethics documentation as required by the Federal Drug Administration (FDA) and other regulatory bodies governing the conduct of the study
• Recruit and screen patients for clinical trials and maintain subject screening and enrollment logs
• Orient research subjects to the study including the purpose of the study, procedures and protocol r...
Work as an integral member of investigator site staff managing the day-to-day coordination and execution of clinical studies in accordance with the protocol, contracted scope of work, good clinical practice, sponsor and standard operating procedures (SOPs) and any relevant local guidelines and regulations.
Essential Functions
• Provide clinical research support to investigators to prepare for and execute assigned research studies
• Review study protocols, source document forms, other study-specific documents, and electronic data capture systems used to record clinical research data
• Collect and submit regulatory/ethics documentation as required by the Federal Drug Administration (FDA) and other regulatory bodies governing the conduct of the study
• Recruit and screen patients for clinical trials and maintain subject screening and enrollment logs
• Orient research subjects to the study including the purpose of the study, procedures and protocol r...