Research Coordinator

Midlands Neurology & Pain Associate S.P.A.; Columbia (SC); On-site; USD 55,000 - 75,000; Full time

Job summary

A medical research facility in Columbia, South Carolina, is seeking a highly organized Clinical Research Coordinator to manage clinical trials while ensuring patient safety and compliance with regulations. Responsibilities include overseeing clinical trial lifecycles and coordinating with various stakeholders. The ideal candidate has 2–3 years of clinical research coordination experience, a relevant bachelor's degree, and strong skills in phlebotomy and patient care. This role offers a unique opportunity to bridge innovative research and compassionate care.

Qualifications

• 2–3 years of experience in clinical research coordination.
• CCRC or CCRP certification is preferred.
• Strong laboratory processing skills.

Responsibilities

• Oversee the lifecycle of clinical trials.
• Screen, enroll, and consent eligible study participants.
• Ensure accurate and timely entry of Case Report Forms (CRFs).
• Perform or coordinate study-related procedures.

Skills

Clinical research coordination

Phlebotomy

Organizational skills

Patient care

Education

Bachelor’s degree in life science or healthcare

Tools

Electronic Data Capture (EDC) systems

Electronic Medical Records (EMR) platforms

Job description

Clinical Research Coordinator

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.