Clinical Trials Support Specialist

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

Job summary

IQVIA in Covington, LA is seeking a Clinical Trial Coordinator to support day-to-day trial activities under regulatory guidelines. The role emphasizes strong organization, communication, and teamwork across study teams and investigators.

You will assist with screening and enrollment, schedule visits, collect participant data, manage data entry, and coordinate lab procedures while ensuring adherence to IRB protocols and SOPs. A High School Diploma is required; a Bachelor's degree is preferred.

Qualifications

• High School Diploma or equivalent is required.
• Bachelor’s Degree is preferred.
• Experience in clinical research coordination is a plus.

Responsibilities

• Develop relationships with study team members and investigators.
• Assist with screening, recruitment and enrollment of subjects.
• Schedule patient visits and manage study visits.
• Collect participant history and perform data entry.
• Coordinate follow-up care and laboratory procedures.
• Adhere to IRB protocols and informed consent process.
• Ensure compliance with SOPs and sponsor policies.

Skills

Interpersonal skills

Team collaboration

Prioritization

Adaptability

Education

High School Diploma or equivalent

Bachelor’s Degree (Pref)

Job description

IQVIA in Covington, LA is seeking a Clinical Trial Coordinator to support day-to-day trial activities under regulatory guidelines. The role emphasizes strong organization, communication, and teamwork across study teams and investigators.

You will assist with screening and enrollment, schedule visits, collect participant data, manage data entry, and coordinate lab procedures while ensuring adherence to IRB protocols and SOPs. A High School Diploma is required; a Bachelor's degree is preferred.