Clinical Research Site Director

Location: Columbia, SC ONSITE
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

• 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

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

  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