Clinical Research Coordinator - 247616

Medix™; Greenville (NC); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

Job summary

A leading clinical research firm in Greenville, NC is seeking a Clinical Research Coordinator. The role involves coordinating patient visits, managing trial activities, and ensuring compliance with research protocols. Ideal candidates have strong organizational and communication skills. The position offers a competitive salary ranging from $60,000 to $75,000 based on experience and full-time employment benefits including medical and vision insurance.

Qualifications

• Experience coordinating clinical trials.
• Familiarity with ICH-GCP guidelines.
• Ability to manage patient interactions.

Responsibilities

• Coordinate daily clinical trial activities.
• Manage inventory of study supplies.
• Train study staff on protocols.
• Create and maintain source documents.
• Attend teleconferences as needed.
• Review study protocols and criteria.
• Work with the team to recruit candidates.

Skills

Organizational skills

Attention to detail

Communication skills

Job description

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

Base pay range

$60,000.00/yr - $75,000.00/yr

Direct message the job poster from Medix™

Clinical Research Recruiter Advisor @ Medix™ | Building relationships within Clinical Research

Seeking a Clinical Research Coordinator in Greenville, NC

Job Title: Research Coordinator

Position Type: Full-Time

Reports To: Clinical Trials Supervisor

Pay: $60,000-75,000 (Depending on experience)

Position Summary

The research coordinator is primarily responsible for coordinating research patient visits according to both the International Council for Harmonisation Good Clinical Practice (ICH‑GCP) guidelines and the Institutional Review Board (IRB)-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.

Duties:

• Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
• Works with team member responsible for ordering study supplies (lab kits, shippers, etc.) to ensure adequate inventory is on hand.
• Ensures study staff is properly trained on study-related information (i.e. protocol, Informed Consent Form [ICF], manuals, etc.) and that the training is documented.
• Creates, manages, and maintains source documents for each trial.
• Attends teleconferences and Investigator Meeting as requested by research director.
• Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.
• Works with other members of the study team and clinical team to recruit eligible candidates to meet enrollment goals.

Seniority level: Not Applicable

Employment type: Full-time

Job function: Research; Industries: Research Services

Referrals increase your chances of interviewing at Medix™ by 2x

Medical insurance

Vision insurance