Research Coordinator

Jobtailor; Charlotte (NC); On-site; USD 52,000 - 74,000; Full time

Job summary

Jobtailor seeks aClinical Research Coordinator to manage trial activities in Charlotte, NC. You will recruit patients, obtain informed consent, coordinate data collection, and ensure regulatory compliance.

The role involves coordinating drug shipments, budget management, and scheduling visits alongside the pharmacy and lab teams. The ideal candidate holds a Bachelor's degree with research experience; a Master's is preferred, and certifications in phlebotomy and clinical research are

Qualifications

• Bachelor's Degree and research experience required
• Master's Degree preferred
• Phlebotomy certification or venipuncture skills preferred
• BLS HCP certification from AHA preferred
• Certification in clinical research (SoCRA, ACRP) preferred

Responsibilities

• Determines protocol-related needs to conduct the trial and orders supplies and equipment
• Recruits and screens potential patients and obtains informed consent
• Assists in providing patient education and explains benefits and risks of participating in a clinical drug trial
• Designs organizational tools and forms to facilitate accurate data collection and recordkeeping
• Conducts in-service programs and summarizes study schedule to aid protocol understanding and implementation
• Manages research funds
• Schedules patient visits and laboratory and diagnostic test procedures
• Coordinates drug shipments, storage, and accountability with pharmacy
• Coordinates with Investigational Pharmacy for subjects to receive required drugs
• Reviews trends, problems encountered, patient adverse events, and patient progress
• Draws blood or collects other samples as needed and eligible

Skills

Patient recruitment

Informed consent

Data collection

Trial coordination

Regulatory compliance

Education

Bachelor's Degree in a related field

Master's Degree preferred

Tools

Phlebotomy certification

BLS HCP certification (AHA)

Clinical research certification (SoCRA/ACRP)

Job description

• Determines protocol-related needs to conduct the trial and orders supplies and equipment
• Recruits and screens potential patients and obtains informed consent
• Assists in providing patient education and benefits and risks of participating in a clinical drug trial
• Designs organizational tools and forms to facilitate accurate data collection and recordkeeping
• Conducts in-service programs, summarizes study schedule to assist in understanding and implementing a protocol
• Manages research funds
• Schedules patient visits and laboratory and diagnostic test procedures
• Coordinates drug shipments, storage, and accountability with pharmacy
• Coordinates with Investigational Pharmacy for subjects to receive required drugs
• Reviews trends, problems encountered, patient adverse events, and patient progress
• Draws blood or collects other samples as needed and eligible

Requirements

• Bachelor's Degree and research experience required
• Master's Degree preferred
• Phlebotomy certification or venipuncture skills preferred
• BLS HCP certification from AHA preferred
• Certification in clinical research (SoCRA, ACRP) preferred

Core Competencies

Demonstrates expertise in clinical trial management, including patient recruitment, informed consent, and data collection. Proficient in coordinating drug shipments and managing research funds while ensuring compliance with clinical research standards.