We are a healthcare-focused research group committed to bringing clinical trials into the communities we serve. Our work bridges the gap between patient care and research innovation by:
Our mission is to improve patient outcomes by integrating research at the point of care.
-
Passionate about patient care and engagement
-
A collaborative team member with a proactive mindset
-
A natural leader with experience managing clinical teams or studies
-
Skilled in all aspects of executing IRB-approved protocols (screening, randomization, visits, documentation)
-
Experienced in direct patient care activities (consenting, assessments, phlebotomy, ECGs, medication administration)
-
Highly detail-oriented and organized—capable of managing regulatory documents, data entry, monitoring visits, and eSource systems
-
An effective communicator who builds strong relationships with PIs, sponsors, CROs, and internal teams
-
Comfortable juggling multiple protocols and regulatory tasks while maintaining focus and quality
-
Inspired by the impact of clinical research in therapeutic areas like Gastroenterology, Urology, Respiratory, Orthopedics, Dermatology, and Oncology
-
Legal authorization to work in the U.S. (no visa sponsorship at this time)
-
RN, LPN, phlebotomy certification or equivalent experience preferred
-
Prior clinical research experience required
Clinical Research Site Director
Location: Columbia, SC
Employment Type: Full-Time
A growing clinical research organization is seeking a Clinical Research Site Director to oversee operations and lead clinical trials at one of our key locations. We’re looking for a dedicated, patient-focused professional with prior clinical research experience and a background in nursing, phlebotomy, or other relevant clinical disciplines.
Who We Are
We are a healthcare-focused research group committed to bringing clinical trials into the communities we serve. Our work bridges the gap between patient care and research innovation by:
-
Expanding access to clinical trials for everyday patients
-
Supporting physicians with enhanced care options
-
Delivering strong clinical trial outcomes for industry sponsors
-
Our mission is to improve patient outcomes by integrating research at the point of care.
Who You Are
-
Passionate about patient care and engagement
-
A collaborative team member with a proactive mindset
-
A natural leader with experience managing clinical teams or studies
-
Skilled in all aspects of executing IRB-approved protocols (screening, randomization, visits, documentation)
-
Experienced in direct patient care activities (consenting, assessments, phlebotomy, ECGs, medication administration)
-
Highly detail-oriented and organized—capable of managing regulatory documents, data entry, monitoring visits, and eSource systems
-
An effective communicator who builds strong relationships with PIs, sponsors, CROs, and internal teams
-
What Success Looks Like
-
Ownership of site performance and study execution
-
Proactive communication with leadership and peers
-
Consistent professionalism and reliability
-
Full compliance with regulatory standards and best practices
-
Willingness to learn and leverage clinical technologies
-
Living out our values of compassion, accountability, collaboration, and innovation
-
What We Offer
-
Competitive compensation
-
401(k) with company match
-
Clear advancement pathway
-
Health, dental, and vision insurance
-
Short- and long-term disability
-
Health Savings & Flexible Spending Accounts
-
Paid time off, paid holidays, and adoption assistance
-
A wide variety of additional voluntary benefits
-
Requirements
-
Legal authorization to work in the U.S. (no visa sponsorship at this time)
-
RN, LPN, phlebotomy certification or equivalent experience preferred
-
Prior clinical research experience required
-
-
Comfortable juggling multiple protocols and regulatory tasks while maintaining focus and quality
-
Inspired by the impact of clinical research in therapeutic areas like Gastroenterology, Urology, Respiratory, Orthopedics, Dermatology, and Oncology
