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Senior Clinical Research Coordinator

Job in Spartanburg, Spartanburg County, South Carolina, 29302, USA
Listing for: Medix™
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 30 - 37.5 USD Hourly USD 30.00 37.50 HOUR
Job Description & How to Apply Below
Position: Senior Clinical Research Coordinator - 246110

Senior Clinical Research Coordinator - 246110

This range is provided by Medix. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Overview

Location:

Spartanburg, South Carolina 29303

Schedule:

M-F 8-5 PM (Contract position through first week of 1/2026 - possibility of full-time hire)

Base pay range: $30.00/hr - $37.50/hr

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
  • 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.

Seniority level
  • Mid-Senior level
Employment type
  • Full-time
Job function
  • Health Care Provider, Research, and Project Management
Industries
  • Hospitals and Health Care, Biotechnology Research, and Research Services

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Position Requirements
10+ Years work experience
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