Contract Virtual Clinical Coordinator

Job not on LinkedIn

🔥 1 minute ago

🏛️ District of Columbia, Washington – Remote

🏛️ District of Columbia – Remote ☕ Washington – Remote

💵 $33k - $82.6k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Conduct remote clinical activities in accordance with study protocols, SOPs, and GCP • Identify, recruit, and virtually enroll eligible patients for clinical trials • Collect, maintain, and securely store clinical research data • Educate potential participants and manage informed consent through virtual interactions • Guide participants and provide reminders to support study compliance • Conduct clinical trial follow-up activities • Monitor participants, report adverse events promptly, and ensure compliance with IRB-approved protocols • Support the research participant call center • Maintain professionalism in participant interactions • Assist with study equipment management, tracking, functionality, and documentation • Communicate updates and provide support to MCRA clinical affairs staff and clients under senior staff guidance • Perform additional duties and projects as assigned

🎯 Requirements

• Bachelor’s degree required (preferably in a life sciences or healthcare-related field) • Minimum of 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 • Knowledge of Standard Operating Procedures (SOPs), Manual of Procedures, and Good Clinical Practice (GCP) • Ability to work weekday hours of 1:00 PM–9:00 PM PST • Ability to work Saturday and/or Sunday, 10:00 AM–6:00 PM PST

🏖️ Benefits

• Potential incentive plans, bonuses, and/or other forms of compensation • Health and welfare and/or other benefits