Clinical research coordinator Jobs in Columbia, SC

Job Description

Summary

The Clinical Research Coordinator (CRC) is responsible for coordinating and executing clinical research studies in compliance with regulatory requirements and institutional guidelines. Additionally, the position will be responsible for maintaining study database, completing study documents, recruiting study patients, and preparing / conducting monitor and auditor visits. The CRC ensures the integrity of study data, subject safety, and protocol adherence while working closely with investigators, sponsors, and clinical teams. Some travel is required.

Entity

Medical University Hospital Authority (MUHA)

Worker Type

Employee

Worker Sub-Type​

Regular

Cost Center

CC005146 COL - Research Service Center - Columbia

Pay Rate Type

Salary

Pay Grade

Health-28

Scheduled Weekly Hours

40

Work Shift

Job Description

Job Title : Clinical Research Coordinator

Location : MUSC Columbia Medical Center Downtown

Entity : MUHA

Worker Type : Employee

Worker Sub-Type :

Pay Rate Type : Non-Exempt

Scheduled Weekly Hours : 40

Job Description

Summary

The Clinical Research Coordinator (CRC) is responsible for coordinating and executing clinical research studies in compliance with regulatory requirements and institutional guidelines. Additionally, the position will be responsible for maintaining study database, completing study documents, recruiting study patients, and preparing / conducting monitor and auditor visits. The CRC ensures the integrity of study data, subject safety, and protocol adherence while working closely with investigators, sponsors, and clinical teams. Some travel is required.

Job Duties

Responsibility

Description

1. Study Coordination & Execution

Coordinate day-to-day operations of assigned clinical trials, including subject recruitment, scheduling, and visit management.

2. Regulatory Compliance & Documentation

Prepare and maintain IRB submissions, regulatory binders, informed consent documents, and other essential documents. Ensure compliance with FDA, GCP, ICH, and institutional policies.

3. Data Collection & Management

Collect, enter, and review study data in case report forms (CRFs) or electronic data capture (EDC) systems. Perform data queries and ensure accuracy and completeness.

4. Participant Interaction & Informed Consent

Conduct informed consent discussions and maintain ongoing communication with participants throughout the study to ensure adherence and safety.

5. Sponsor & Monitor Communication

Liaise with sponsors, CROs, and monitors during site initiation, monitoring visits, and close-outs. Ensure timely query resolution and protocol adherence.

6. Training & Education

Stay current with regulatory requirements and clinical research practices. Participate in ongoing training and continuing education. May assist in training new staff.

7. Budget & Financial Tracking

Support budget development and track participant stipends and study-related billing. Communicate with finance teams as needed.

8. Other Duties as Required

Other duties as assigned

Qualifications –

Bachelor’s degree in a health-related field or equivalent combination of education and experience; Bachelor RN preferred but not required.

Working knowledge of GCP, FDA regulations, and clinical trial operations

Familiarity with medical terminology, HIPAA, or Good Clinical Practice (GCP)

Excellent communication, organization, and interpersonal skills

Ability to collect, organize and analyze information in a clear and concise manner

Proficiency with EDC systems, Microsoft Office Suite, and medical terminology

Additional Knowledge and Skills Preferred

Minimum 1–2 years of experience in clinical research coordination preferred

Prior exposure to clinical research in an academic, hospital, or lab setting (through coursework, volunteering, or work-study)

Laboratory or phlebotomy experience is preferred but not required

Certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA) is a plus

Working Conditions

Standard office and clinical setting

May require occasional travel to satellite locations or sponsor meetings

Must be able to work flexible hours to accommodate patient schedules or protocol requirements

Additional

Job Description

Qualifications –

Bachelor’s degree in a health-related field or equivalent combination of education and experience; Bachelor RN preferred but not required.

Working knowledge of GCP, FDA regulations, and clinical trial operations

Familiarity with medical terminology, HIPAA, or Good Clinical Practice (GCP)

Excellent communication, organization, and interpersonal skills

Ability to collect, organize and analyze information in a clear and concise manner

Proficiency with EDC systems, Microsoft Office Suite, and medical terminology

Additional Knowledge and Skills Preferred

Minimum 1–2 years of experience in clinical research coordination preferred

Prior exposure to clinical research in an academic, hospital, or lab setting (through coursework, volunteering, or work-study)

Laboratory or phlebotomy experience is preferred but not required

Certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA) is a plus

If you like working with energetic enthusiastic individuals, you will enjoy your career with us!

The Medical University of South Carolina is an Equal Opportunity Employer. MUSC does not discriminate on the basis of race, color, religion or belief, age, sex, national origin, gender identity, sexual orientation, disability, protected veteran status, family or parental status, or any other status protected by state laws and / or federal regulations. All qualified applicants are encouraged to apply and will receive consideration for employment based upon applicable qualifications, merit and business need.

Medical University of South Carolina participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here : http : / / www.uscis.gov / e-verify / employees