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Clinical Research Coordinator - 246110

Clinical Research Coordinator - 246110

MedixSpartanburg, SC, United States
1 day ago
Job type
  • Full-time
Job description

Job Title : Clinical Research Coordinator I (Contract through Jan 2026)

Employment Type : Contract (with potential for permanent hire)

Schedule : Monday–Friday, 8 AM–5 PM | Flexibility for occasional evenings / weekends required

Pay Range : Based on experience

Location : Spartanburg, South Carolina 29303

About the Role :

We’re seeking a Clinical Research Coordinator I (CRC I) for a full-time contract position through January 2026 , with the potential for a performance-based review and possible transition to a permanent role. This is a unique opportunity to contribute to innovative clinical research while growing your career in a fast-paced, mission-driven environment.

As a CRC I, you will help manage and conduct clinical trials from start-up to close-out, ensuring adherence to protocol, GCP guidelines, and internal SOPs—all while delivering high-quality data and excellent patient care.

What You’ll Do :

  • Coordinate and conduct clinical trials under supervision
  • Recruit and screen study participants
  • Perform study visits and collect source documentation
  • Ensure timely and accurate data entry and resolution of queries
  • Handle adverse event reporting and protocol amendments
  • Maintain regulatory compliance and documentation
  • Communicate with sponsors, CROs, vendors, and site staff
  • Perform select clinical procedures within scope (e.g., phlebotomy, ECG, drug prep / admin)

Qualifications :

  • Bachelor's degree + 1 year of relevant life sciences experience
  • OR Associate’s degree + 2 years relevant experience
  • OR High school diploma + 3 years relevant experience
  • Phlebotomy certification if required by state law
  • Strong organizational, communication, and multitasking skills
  • Comfortable with fast-paced environments and evolving schedules
  • Clinical research experience preferred
  • Preferred Skills :

  • Familiarity with GCP / ICH guidelines
  • Experience using clinical data systems and Microsoft Office
  • Excellent documentation practices and attention to detail
  • Ability to work independently and as part of a team
  • Strong problem-solving and critical thinking abilities
  • Physical Requirements :

  • Ability to sit / stand for extended periods
  • Lift up to 30 lbs
  • Local and occasional national travel may be required
  • Why Apply?

    While this is a contract role through early January 2026, high-performing candidates may be considered for extension or permanent placement. You’ll have the chance to be part of a passionate, purpose-driven team that supports professional growth and makes a meaningful impact in healthcare.

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    Clinical Research Coordinator • Spartanburg, SC, United States