Medix™
Senior Clinical Research Coordinator - 246110
Medix™, Spartanburg, South Carolina, United States, 29302
Senior Clinical Research Coordinator
Location: Spartanburg South Carolina 29303
Schedule: M-F 8-5 PM (Contract position through first week of 1/2026 - possibility of full time hire)
Compensation: Based on experience
We are seeking an experienced
Senior Clinical Research Coordinator
to lead clinical trial operations at our integrated research site. This is a temporary, full-time, on-site position ideal for someone passionate about clinical research, patient care, and operational excellence. You’ll serve as the subject matter expert and team leader responsible for managing trials from start-up through close-out.
What You'll Do As a Senior Clinical Research Coordinator, you will: Lead clinical trial teams and serve as the primary point of contact for assigned studies Conduct studies in compliance with GCP, ICH guidelines, protocol, and SOPs Train and mentor junior staff in protocol requirements, documentation, and communication Oversee subject recruitment, scheduling, source documentation, and data entry Manage adverse event reporting, deviations, and protocol amendments Collaborate with sponsors, CROs, vendors, and internal stakeholders Create and execute quality control and risk mitigation strategies Maintain regulatory compliance with all required documentation and reporting Perform clinical tasks within scope (e.g., phlebotomy, ECGs, lab processing) Uphold confidentiality and patient safety across all study processes
Minimum Qualifications: Bachelor’s degree + 4 years of experience as a Clinical Research Coordinator OR Associate’s degree + 6 years of experience OR High school diploma/technical degree + 8 years of experience
Certifications (Required or within 6 months): Certified Clinical Research Coordinator (ACRP or SOCRA) Phlebotomy and IV/IM administration certification if required by state law
Key Skills: Advanced knowledge of medical terminology and clinical research practices Strong leadership, mentorship, and project management abilities Excellent verbal and written communication skills Proficiency with Microsoft Office and clinical data systems Ability to multitask, prioritize, and adapt in a fast-paced environment Detail-oriented with strong problem-solving and decision-making capabilities
Physical Requirements: Ability to sit or stand for extended periods Local and national travel as needed Ability to lift up to 30 lbs occasionally
What We Offer Competitive compensation Medical, dental, and vision coverage Paid time off and company holidays 401(k) with company match Annual performance-based incentive program Opportunities for growth and development in clinical research
Apply Today If you’re a driven, detail-oriented clinical research professional ready to take on a leadership role, we encourage you to apply. Join a team dedicated to advancing medical innovation while delivering exceptional patient care.
We are seeking an experienced
Senior Clinical Research Coordinator
to lead clinical trial operations at our integrated research site. This is a temporary, full-time, on-site position ideal for someone passionate about clinical research, patient care, and operational excellence. You’ll serve as the subject matter expert and team leader responsible for managing trials from start-up through close-out.
What You'll Do As a Senior Clinical Research Coordinator, you will: Lead clinical trial teams and serve as the primary point of contact for assigned studies Conduct studies in compliance with GCP, ICH guidelines, protocol, and SOPs Train and mentor junior staff in protocol requirements, documentation, and communication Oversee subject recruitment, scheduling, source documentation, and data entry Manage adverse event reporting, deviations, and protocol amendments Collaborate with sponsors, CROs, vendors, and internal stakeholders Create and execute quality control and risk mitigation strategies Maintain regulatory compliance with all required documentation and reporting Perform clinical tasks within scope (e.g., phlebotomy, ECGs, lab processing) Uphold confidentiality and patient safety across all study processes
Minimum Qualifications: Bachelor’s degree + 4 years of experience as a Clinical Research Coordinator OR Associate’s degree + 6 years of experience OR High school diploma/technical degree + 8 years of experience
Certifications (Required or within 6 months): Certified Clinical Research Coordinator (ACRP or SOCRA) Phlebotomy and IV/IM administration certification if required by state law
Key Skills: Advanced knowledge of medical terminology and clinical research practices Strong leadership, mentorship, and project management abilities Excellent verbal and written communication skills Proficiency with Microsoft Office and clinical data systems Ability to multitask, prioritize, and adapt in a fast-paced environment Detail-oriented with strong problem-solving and decision-making capabilities
Physical Requirements: Ability to sit or stand for extended periods Local and national travel as needed Ability to lift up to 30 lbs occasionally
What We Offer Competitive compensation Medical, dental, and vision coverage Paid time off and company holidays 401(k) with company match Annual performance-based incentive program Opportunities for growth and development in clinical research
Apply Today If you’re a driven, detail-oriented clinical research professional ready to take on a leadership role, we encourage you to apply. Join a team dedicated to advancing medical innovation while delivering exceptional patient care.