Lead Clinical Research Coordinator (Medical Devices)

Location: Washington, DC, United States of America

Annual base pay: $49,200–$123,000

Company

IQVIA MedTech and MCRA provide clinical research, regulatory, market access, and post-market services for the medical device and diagnostics industry.

What you will do

• Coordinate and perform remote clinical activities in compliance with study protocols, SOPs, GCP, and Manuals of Procedures.
• Collaborate with research teams and study sites to identify, recruit, and virtually enroll eligible clinical trial participants.
• Educate participants about study requirements and manage informed consent through virtual interactions.
• Collect, maintain, securely store, and report clinical trial data in line with regulatory and organizational standards.
• Monitor participant safety, support protocol adherence, conduct follow-ups, and promptly report adverse events.
• Support the participant call center, study equipment management, and communication with clinical affairs staff and clients.

Requirements

• Bachelor’s degree required, preferably in life sciences or a healthcare-related field.
• At least three years of experience as a Clinical Coordinator or in a comparable clinical research role.
• Strong attention to detail.
• Excellent verbal and written communication skills.
• Working knowledge of study-specific software applications and equipment.
• Ability to follow GCP, SOPs, and IRB-approved protocols.

Culture & Benefits

• Work within a global clinical research and healthcare intelligence organization.
• Support innovation across the medical device and diagnostics lifecycle.
• Health and welfare benefits may be provided.
• Incentive plans, bonuses, or other compensation may be available depending on the position.