Clinical Trial Research Assistant - Study Coordination & Data

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

Job summary

IQVIA is seeking an individual to support clinical trial activities, including coordinating visits, screening and enrolling participants, and managing data in compliance with regulations. You will build strong relationships with study teams, investigators, and office staff to ensure smooth trial operations.

The role emphasizes adherence to IRB protocols, informed consent support, patient safety, and collaboration across the research office to coordinate procedures and follow-up care in a

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 trust between the clinic and research office.
• Assist with 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, 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 support clinical trial activities, including coordinating visits, screening and enrolling participants, and managing data in compliance with regulations. You will build strong relationships with study teams, investigators, and office staff to ensure smooth trial operations.

The role emphasizes adherence to IRB protocols, informed consent support, patient safety, and collaboration across the research office to coordinate procedures and follow-up care in a