Clinical Research Assistant — Trial Coordination

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

Job summary

IQVIA is seeking a detail-oriented professional to assist in conducting clinical trial activities in compliance with all applicable regulations. The role emphasizes building strong relationships with study teams, investigators, and clinic staff, while coordinating subject screening, enrollment, and scheduling.

Essential functions include data management, protocol adherence, informed consent support, and coordination of lab procedures, with emphasis on patient safety and SOP compliance.

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 clinic and research office.
• Assist with screening, recruiting and enrollment of research subjects.
• Schedule patient/research participant visits and procedures.
• 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 and study visits.
• Comply with SOPs and guidelines.

Skills

Logical thinking

Prioritization

Adaptability

Interpersonal skills

Team building

Education

High School Diploma or equivalent

Bachelor's Degree

Job description

IQVIA is seeking a detail-oriented professional to assist in conducting clinical trial activities in compliance with all applicable regulations. The role emphasizes building strong relationships with study teams, investigators, and clinic staff, while coordinating subject screening, enrollment, and scheduling.

Essential functions include data management, protocol adherence, informed consent support, and coordination of lab procedures, with emphasis on patient safety and SOP compliance.