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Job summary
A healthcare research firm in Clinton Charter Township, MI is seeking a Clinical Research Coordinator (CRC) to manage clinical trials and support research studies. The ideal candidate will have a Bachelor's degree, preferably with 2+ years of clinical research experience, and certifications in Phlebotomy or Medical Assistance. Responsibilities include participant recruitment, data collection, compliance, and communication with sponsors. This full-time position demands exceptional organizational and communication skills in a team-oriented environment.
Qualifications
2+ years of experience in clinical research preferred.
State Phlebotomy license required.
MA certification preferred.
Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
Responsibilities
Coordinate day-to-day clinical research activities to ensure study protocols are followed.
Recruit, screen, and enroll study participants.
Obtain informed consent and ensure ethical conduct in all study interactions.
Collect, process, and ship biological specimens per protocol.
Perform basic clinical procedures as permitted by certification.
Skills
Organizational skills
Interpersonal skills
Communication skills
Proficiency in Microsoft Office
Education
Bachelor's degree in a health-related field
Tools
REDCap
EDC platforms
Job description
A healthcare research firm in Clinton Charter Township, MI is seeking a Clinical Research Coordinator (CRC) to manage clinical trials and support research studies. The ideal candidate will have a Bachelor's degree, preferably with 2+ years of clinical research experience, and certifications in Phlebotomy or Medical Assistance. Responsibilities include participant recruitment, data collection, compliance, and communication with sponsors. This full-time position demands exceptional organizational and communication skills in a team-oriented environment.