Clinical Trial Research Associate

IQVIA; Covington (KY); On-site; USD 30,000 - 76,000; Full time

Job summary

IQVIA is seeking an individual to assist in clinical trial activities in compliance with regulations. The role emphasizes adaptability, teamwork, and strong interpersonal skills to support study teams, investigators, and office staff.

Key duties include screening and enrolling subjects, scheduling visits, data entry, and ensuring adherence to IRB protocols while maintaining subject safety throughout the study process.

Qualifications

• High school diploma or equivalent required.
• Bachelor's degree preferred.

Responsibilities

• Develop strong working relationships and maintain effective communication with study team members
• Develop strong working relationships with investigators and office staff to build a foundation of trust and respect between the clinic and the research office
• Assists with the screening, recruiting and enrollment of research subjects
• Perform patient/research participant scheduling
• Collect patient/research participant history
• Data entry and management
• Coordinate follow up care and laboratory procedures
• Adhere to an IRB approved protocol
• Assist in the informed consent process of research subjects
• Support the safety of research subjects
• Coordinate protocol related research procedures, study visits, and follow up care
• Comply with company and Sponsor policies, standard operating procedures (SOPs) and guidelines
• Schedule subject visits and procedures

Education

High School Diploma or equivalent

Bachelor's Degree

Job description

IQVIA is seeking an individual to assist in clinical trial activities in compliance with regulations. The role emphasizes adaptability, teamwork, and strong interpersonal skills to support study teams, investigators, and office staff.

Key duties include screening and enrolling subjects, scheduling visits, data entry, and ensuring adherence to IRB protocols while maintaining subject safety throughout the study process.