CRA: Frontline Site Monitor Driving Trial Impact

Parexel; Honolulu (HI); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Health Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending & Health Savings

Work/Life Balance

401(k) with Company match

Pet Insurance

Job summary

Parexel is seeking a Clinical Research Associate with at least 12 months of on-site monitoring experience to manage clinical sites from initiation to closeout. In this role you will ensure study quality, patient safety, regulatory compliance, and accurate data while building productive relationships with site teams.

You will conduct visits, support enrollment, and oversee data integrity across sites, contributing to high-quality clinical research delivery and patient-focused trials.

Qualifications

• Minimum 12 months of on-site CRA monitoring experience.
• Bachelor’s degree or equivalent in biological science, pharmacy, or health-related field.
• Knowledge of GCP and regulatory requirements; familiarity with trial processes.
• Experience using CTMS/EDMS and MS Office applications.
• Strong interpersonal, written, verbal, organizational, and problem-solving skills.
• Oncology, ophthalmology, CAR-T, or MASH trial monitoring experience preferred.

Responsibilities

• Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned sites and prepare reports.
• Manage site quality and delivery from site identification through closeout.
• Serve as primary contact for sites, addressing questions and resolving issues to support study execution.
• Monitor study integrity and build relationships with investigators and site staff.
• Review trial performance to safeguard participant rights and safety.

Skills

Site monitoring

CRA

GCP knowledge

Regulatory compliance

Study coordination

Communication

Education

Bachelor’s degree in biological science or health-related discipline

Tools

CTMS

EDMS

Microsoft Office (Excel, Word)

Job description

Parexel is seeking a Clinical Research Associate with at least 12 months of on-site monitoring experience to manage clinical sites from initiation to closeout. In this role you will ensure study quality, patient safety, regulatory compliance, and accurate data while building productive relationships with site teams.

You will conduct visits, support enrollment, and oversee data integrity across sites, contributing to high-quality clinical research delivery and patient-focused trials.