Research Coordinator

Midlands Neurology & Pain Associates; Columbia (SC); On-site; USD 55,000 - 75,000; Full time

Job summary

A medical research organization in Columbia, South Carolina, is seeking a skilled Clinical Research Coordinator. This role involves managing the daily operations of clinical trials, ensuring compliance with regulations, and maintaining high patient safety standards. Ideal candidates should have 2–3 years of experience in clinical research coordination and a Bachelor’s degree in a relevant field. CCRC or CCRP certification is preferred. Strong organizational skills and proficiency with EDC systems are essential.

Qualifications

• 2–3 years of experience in clinical research coordination.
• Bachelor’s degree in a life science, healthcare, or related field is required.
• CCRC or CCRP certification is highly preferred.

Responsibilities

• Oversee the lifecycle of clinical trials from site initiation to close-out.
• Screen and enroll eligible study participants and maintain retention.
• Ensure timely entry of Case Report Forms and maintain regulatory binders.

Skills

Clinical trial management

Patient recruitment and retention

Data entry and regulatory compliance

Phlebotomy

Organizational skills

Education

Bachelor’s degree in a life science or related field

CCRC or CCRP certification

Tools

Electronic Data Capture (EDC) systems

Electronic Medical Records (EMR) platforms

Job description

Seeking a highly organized, detail-oriented Clinical Research Coordinator to join our team and bridge the gap between innovative medical research and compassionate patient care.

As the Clinical Research Coordinator, you will manage the daily operations of our clinical trials. You will work closely with our Principal Investigators (PIs), clinical staff, and industry sponsors to ensure that all research is conducted with the highest degree of integrity, compliance, and patient safety.

Key Responsibilities

• Oversee the lifecycle of clinical trials from site initiation to close-out.
• Screen, enroll, and consent eligible study participants; maintain high retention rates through excellent communication.
• Ensure accurate and timely entry of Case Report Forms (CRFs) and maintain meticulous regulatory binders.
• Adhere strictly to ICH-GCP guidelines, HIPAA regulations, and study-specific protocols.
• Perform or coordinate study-related procedures (vitals, phlebotomy, ECGs, and sample processing).
• Serve as the primary point of contact for Clinical Research Associates (CRAs) during monitoring visits and audits.

Qualifications

• Minimum of 2–3 years of experience in clinical research coordination.
• Bachelor’s degree in a life science, healthcare, or related field.
• CCRC or CCRP (ACRP/SoCRA) certification is highly preferred.
• Proficiency with Electronic Data Capture (EDC) systems and EMR platforms.
• Strong phlebotomy and laboratory processing skills.
• Exceptional organizational skills with the ability to manage multiple protocols simultaneously.
• Professional demeanor, high ethical standards, and a "patient-first" mentality.