SQRL
Highlights
$70,000 - $80,000 based on exp
Great benefits
Consistent schedule, no overnights or weekends
Work with unique studies in psychedelic research, CNS, Neurology, and more
Apply promptly! A high volume of applicants is expected for the role as detailed below, do not wait to send your CV.
About Our Client With a mission to advance research, our client is a privately held network of research sites in South Florida conducting Phase I-IV research trials in psychiatry, neurology, addiction, insomnia, general medicine, vaccines, women’s health, and more. To date, they have been an instrumental part in conducting studies resulting in many medications and devices that are FDA approved and are changing the quality of life for millions! They are a cutting edge company.
Responsibilities As a CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process!
Conduct procedures such as vital signs, blood draws, EKGs, and bladder scans. Patient recruitment, enrollment, scheduling, and consent Lab procedures and shipments Maintain GCP and follow protocols AE/SAE reporting Data management in EDC systems Overall coordination of the study Some regulatory work as needed
Qualifications: 4+ years of experience working as a CRC on sponsor backed clinical trials Phlebotomy and lab processing experience (ability to perform without supervision) Ability to work on site M-F on site (there is no remote or hybrid days)
Apply promptly! A high volume of applicants is expected for the role as detailed below, do not wait to send your CV.
About Our Client With a mission to advance research, our client is a privately held network of research sites in South Florida conducting Phase I-IV research trials in psychiatry, neurology, addiction, insomnia, general medicine, vaccines, women’s health, and more. To date, they have been an instrumental part in conducting studies resulting in many medications and devices that are FDA approved and are changing the quality of life for millions! They are a cutting edge company.
Responsibilities As a CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process!
Conduct procedures such as vital signs, blood draws, EKGs, and bladder scans. Patient recruitment, enrollment, scheduling, and consent Lab procedures and shipments Maintain GCP and follow protocols AE/SAE reporting Data management in EDC systems Overall coordination of the study Some regulatory work as needed
Qualifications: 4+ years of experience working as a CRC on sponsor backed clinical trials Phlebotomy and lab processing experience (ability to perform without supervision) Ability to work on site M-F on site (there is no remote or hybrid days)