What are the responsibilities and job description for the Clinical Research Coordinator - 255152 position at Medix™?
Clinical Research Coordinator
Must Haves: 2 years of CRC experience, high school diploma minimum required, basic clinical skills (vitals, EKGs) required.
Hours: 40 hours per week, Monday-Thursday 8am-5pm, Friday half days from 8am-12pm but are more than welcome to work a full day if you wanted to.
Contract Duration: Permanent position
Benefits: Medical, Dental, Vision, time off, paid holidays off, 401k, growth opportunities, etc.
Position Summary
We're looking for a motivated, organized, and patient-focused Clinical Research Coordinator to join our clinical research team.
This position supports the successful execution of clinical trials through participant management, protocol compliance, sponsor communication, and accurate study documentation. Candidates with strong clinical experience may begin as a Clinical Research Assistant while completing Del Sol Research's internal training program before progressing into the Clinical Research Coordinator role.
The ideal candidate is detail-oriented, adaptable, and committed to delivering exceptional participant care while maintaining the highest standards of research quality and regulatory compliance.
Key Responsibilities
- Coordinate clinical research studies across multiple therapeutic areas.
- Assist investigators with all aspects of assigned research protocols.
- Support study start-up activities, site initiation, and participant enrollment strategies.
- Prepare source documents and study visit materials.
- Recruit, screen, schedule, enroll, and follow participants throughout each study.
- Obtain informed consent under investigator supervision.
- Coordinate laboratory, diagnostic, and study-specific procedures.
- Maintain accurate source documentation and electronic case report forms (eCRFs).
- Communicate with sponsors, monitors, investigators, and participants.
- Schedule and host monitoring visits, audits, and sponsor meetings.
- Identify, document, and report adverse events and protocol deviations.
- Prepare, process, and ship laboratory specimens per protocol.
- Maintain protocol compliance and participant safety.
- Assist with training Clinical Research Assistants as assigned.
- Attend investigator meetings and sponsor trainings.
- Perform additional research-related duties as assigned.
Apply Today!
Salary : $25 - $30