Clinical Research Coordinator

Responsibilities

• Perform a variety of clinical procedures, including ECG, sample collection, and vital signs
• Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines
• Support study conducts by preparing study materials, setting up equipment, and planning logistical activities
• Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study
• Collect and accurately record clinical data in case report forms (CRFs)
• Collaborate with investigators and monitors, addressing queries and ensuring data quality
• Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies

Preferred

• Bachelor's degree preferred or equivalent combination of education and relevant experience

Benefits

• Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
• Glassdoor
• 3.9
• IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
• Durham, North Carolina, USA
• https://www.iqvia.com
• Public Company
• Total Funding
• $6.61B
• 2026-09-09
• Post Ipo Debt· $2B
• 2026-06-04
• Post Ipo Debt· $1.11B
• 2025-06-02
• Leadership Team
• Karl Guenault
• SVP and Chief Information Officer
• Chris Colapietro
• Vice President, Customer Engagement
• Recent News
• PR Newswire UK
• IQVIA Selects Veeva Clinical Operations Applications
• 2026-10-16
• FierceBiotech
• IQVIA, Veeva expand on existing partnership for speedier clinical trials
• BioSpace
• IQVIA Launches IQVIA Life Science Models to Help Life Sciences Companies Predict Clinical Trial Outcomes
• 2026-10-08
• Company data provided by
• AI Tools

Qualifications

• Minimum 1+ years of relevant work experience in clinical research
• Working knowledge of clinical trials, GCP principles, and medical terminology
• Strong attention to detail and ability to establish effective working relationships
• Proficiency with **EDC systems**, data entry accuracy, and query management
• Bachelor's degree preferred or equivalent combination of education and relevant experience
• Minimum 1+ years of relevant work experience in clinical research.

Required skills

• Clinical Practice (GCP), Clinical Research, Clinical Trials, Data Entry, EDC Systems, Medical Terminology, Query Management

Experience

• 1+ years