Medix™
Clinical Research Coordinator - 246110
Medix™, Spartanburg, South Carolina, United States, 29302
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.
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.