Senior Clinical Research Coordinator - 246110

Medix™; Spartanburg (SC); On-site; USD 41,328 - 51,660; Full time

Benefits offered by this job

Medical, dental, and vision coverage

401(k) with company match

Paid time off and company holidays

Opportunities for growth and development

Job summary

A leading clinical research organization in Spartanburg is seeking a Senior Clinical Research Coordinator to oversee clinical trials and manage research teams. This full-time position requires strong leadership skills and a background in clinical research. The ideal candidate will have excellent communication skills and the ability to navigate fast-paced environments. Competitive compensation and opportunities for professional growth are offered.

Qualifications

• Experience in clinical research coordination required.
• Certification in Clinical Research Coordinator must be obtained within 6 months.
• Ability to meet physical requirements like standing for long periods.

Responsibilities

• Lead clinical trial teams and manage studies.
• Ensure compliance with GCP and ICH guidelines.
• Train junior staff on protocol and documentation.

Skills

Medical terminology knowledge

Leadership ability

Project management skills

Excellent communication

Microsoft Office proficiency

Education

Bachelor's degree + 4 years of experience

Associate's degree + 6 years of experience

High school diploma/technical degree + 8 years of experience

Job description

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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