Clinical Research Coordinator

Job overview

The Clinical Research Coordinator works 100% onsite in Walhalla, SC, for an expected 20 hours per week. Compensation is $30–$36 per hour. SiteBridge Research’s network connects community practices with sponsored clinical research, including communities with unmet health needs. The coordinator supports the Principal Investigator and clinical staff in daily trial operations. By coordinating participants, study documentation, and protocol and regulatory compliance, the role helps studies run efficiently and reach timely completion. Travel of up to 25% may be needed.

What you'll do

• Communicate with participants about study objectives
• administer questionnaires and monitor protocol compliance
• oversee study activities for protocol and regulatory adherence
• maintain study and staff records
• screen and recruit participants, schedule visits, obtain informed consent, and conduct intake assessments
• track enrollment
• prepare trial documents and reports
• maintain essential study records
• update the PI and site operations leads on study progress
• travel up to 25% as needed.

What we're looking for

Skills & competencies

clinical research coordinator

clinical trials

study operations

participant recruitment

informed consent

ich/gcp

fda compliance

walhalla sc

part-time

20 hours per week

up to 25% travel

$30–$36/hr

sitebridge research

Work arrangement

• Weekend coverage required

Why this role

Part-time role with an expected 20-hour workweek; travel up to 25% as needed; requires a relevant life-science bachelor’s degree, three or more years of clinical trial experience, and FDA and ICH/GCP knowledge.

About the employer

SiteBridge Research, Inc. is hiring for this role. Industry: Offices of Physicians (except Mental Health Specialists). Sector: 62.