Remote Clinical Trial Coordinator — 6-Month Contract

IQVIA; United States; Remote; USD 33,000 - 83,000; Full time

Job summary

IQVIA is seeking a Contract Virtual Clinical Coordinator to support clinical studies through remote activities in line with study protocols and Good Clinical Practice. The role involves collecting and interpreting patient data, coordinating with sites, and ensuring SOP compliance.

Requirements include a Bachelor’s degree in life sciences or healthcare field and at least three years of experience as a Clinical Coordinator.

Qualifications

• Bachelor’s degree in life sciences or healthcare field.
• Minimum of three years as Clinical Coordinator or similar role.
• Strong attention to detail and communication skills.

Responsibilities

• Adhere to SOPs and MOPs during study activities to ensure compliance.
• Collaborate with research team and sites to recruit and enroll patients remotely.
• Collect, maintain, and securely store data per regulatory standards.
• Educate participants about trials and manage the informed consent process remotely.
• Assist with participant study compliance and provide guidance to ensure protocol adherence.
• Conduct follow-up activities and ensure alignment with GCP guidelines.
• Monitor participant safety and report adverse events per IRB protocols.
• Support the research participant call center and assist with inquiries.
• Maintain professionalism in all interactions with participants.
• Assist with study equipment management and reporting.
• Communicate effectively with MCRA staff and clients under guidance of senior staff.
• Perform additional duties to support clinical research operations.

Skills

Attention to detail

Communication skills

Clinical data entry

Education

Bachelor’s degree

Job description

IQVIA is seeking a Contract Virtual Clinical Coordinator to support clinical studies through remote activities in line with study protocols and Good Clinical Practice. The role involves collecting and interpreting patient data, coordinating with sites, and ensuring SOP compliance.

Requirements include a Bachelor’s degree in life sciences or healthcare field and at least three years of experience as a Clinical Coordinator.