Clinical Research Coordinator: Drive Trials & Data Excellence
ECN Operating LLC
Crystal City (MO)
On-site
USD 50,000 - 70,000
Full time
14 days+
Application generator
Don’t send a generic resume — generate a resume and cover letter tailored to this exact role.
Get past ATS filters
Job summary
ECN Operating LLC is seeking a Clinical Research Coordinator (CRC) in Crystal City, Missouri, to manage various aspects of clinical trials. The CRC will handle participant recruitment, data collection, and regulatory compliance while ensuring adherence to ethical standards. Required qualifications include a Bachelor's degree in a health-related field and preferred certifications in Phlebotomy or as a Medical Assistant. Strong organizational and communication skills are essential, and proficiency in electronic data systems such as REDCap is desired.
Qualifications
1-2 years of experience in clinical research preferred.
Phlebotomy certification or Medical Assistant certification preferred.
Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
Responsibilities
Coordinate clinical research activities to ensure protocols are followed.
Recruit, screen, and enroll study participants.
Maintain documentation in case report forms and electronic databases.
Skills
Organizational skills
Communication skills
Detail-oriented
Microsoft Office proficiency
Data collection
Education
Bachelor's degree in a health-related field
Tools
REDCap
EDC platforms
Job description
ECN Operating LLC is seeking a Clinical Research Coordinator (CRC) in Crystal City, Missouri, to manage various aspects of clinical trials. The CRC will handle participant recruitment, data collection, and regulatory compliance while ensuring adherence to ethical standards. Required qualifications include a Bachelor's degree in a health-related field and preferred certifications in Phlebotomy or as a Medical Assistant. Strong organizational and communication skills are essential, and proficiency in electronic data systems such as REDCap is desired.