Clinical Research Coordinator - Phlebotomist

Benefits

Qualifications

• •Must be willing to work a flexible schedule as necessary to meet deadlines

Responsibilities

• •The CRC will be responsible for coordinating clinical research studies
• •They will be responsible for studies from start up to close out
• •This candidate will work closely with Principal Investigator (PI) and Sub-investigators as well as other CRCs, Research Fellows and research assistants
• •Specific duties will include recruiting and screening study subjects and overseeing study visit procedures in accordance with FDA Regulations and Good Clinical Practices
• •ISSR operates Monday through Friday | 8:30am - 5:00pm
• •Organize and run clinical studies
• •Actively recruit participants
• •Calling and following up with potential research patients to inform them about research studies and assess patient interest
• •Manage of and perform clinical study procedures such as blood draws, maintenance of regulatory binders up to date, update data collection databases and answer queries in a timely fashion
• •Perform laboratory processing as needed for study protocols and organize shipments of labs in a timely fashion
• •Maintaining accurate and complete study records by FDA regulations as well as sponsor/CRO and IRB regulations and guidance, study records
• •Communicate with study monitors and organize responses and queries to monitoring visit reviews
• •Proactively focus on clinical trial organization
• •Keep invoices up to date for studies and to make sure you have the unit ready for internal and external audits
• •Assist with other needs in the clinical trials unit as they arise and/or as directed by your supervisors
• •Other duties as assigned or directed by the site manager and director
• •13 more items(s)