Contract - Clinical Research Coordinator

The role

The Clinical Research Coordinator recruits, enrolls, and conducts follow-up of study participants in clinical trials. This role involves coordinating trial participation in compliance with protocols, SOPs, GCP, and FDA regulations.

What you will do

• Implement and execute clinical trial activities from start-up to closure
• Attend and lead investigator, project, and department meetings
• Participate as temporary Project Manager for smaller studies as needed
• Enlist and maintain protocol compliance for study participants
• Collaborate with investigators to determine participant eligibility
• Screen potential participants and participate in the informed consent process
• Ensure research quality through compliance with SOPs, GCP, and regulations
• Support development and distribution of clinical protocols and study documents
• Coordinate patient care and maintain investigational drug accountability
• Collect, document, enter, and report data accurately and timely

Required qualifications

• Minimum of 5 years of pharmaceutical-sponsored clinical research experience or commensurate education, training, and experience
• Experience working with patients in a HIPAA regulated environment
• Knowledge of good clinical practice (GCP) and applicable regulatory requirements
• Ability to conduct collaborative interaction with cross functional team members
• Proficient with MS Office and Google Suite applications
• Ability to communicate in English (both verbal and written)

Nice to have

• Bachelor's degree
• Advanced degree
• ACRP (CCRC) or SoCRA (CCRP) certification
• Medical and scientific knowledge

About the company

Science 37 accelerates clinical research by expanding patient access to trials. Their solutions empower life sciences companies to reach diverse populations.