Remote CRA - Site Monitoring & Study Quality

Parexel; United States; Remote; USD 70,000 - 100,000; Full time

Benefits offered by this job

Health Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending & Health Savings

401(k) with Company match

Pet Insurance

Job summary

Parexel is seeking a Clinical Research Associate (CRA) with at least 12 months of onsite monitoring experience to manage clinical sites from initiation through closeout. You will ensure study quality, patient safety, regulatory compliance, and accurate data across multiple therapeutic areas.

You will conduct onsite visits, maintain site relationships, address issues, and support enrollment and study delivery.

Qualifications

• Bachelor's degree or equivalent in biological science, pharmacy, or another health-related discipline.
• Knowledge of Good Clinical Practice and regulatory requirements.
• Experience with clinical trial processes and site monitoring.

Responsibilities

• Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned sites.
• Manage site quality and delivery from site identification through closeout.
• Serve as primary contact for assigned clinical sites and address questions to support study execution.
• Oversee study integrity and build relationships with investigators and site staff.
• Review trial performance and safeguard participant rights, safety, and well-being.
• Develop patient recruitment strategies with sites to support enrollment timelines.
• Ensure compliance with SOPs, protocols, GCP, and regulatory requirements.
• Evaluate data quality and site documentation; perform site document verification.

Skills

Site relationship management

Problem-solving

Communication skills

Independent work with urgency

Client-focused approach

Multi-priority management

Attention to quality & detail

Matrixed team collaboration

Education

Bachelor's degree or equivalent in biological science, pharmacy, or health-related discipline

Tools

Clinical Trial Management System

Electronic Document Management System

Microsoft Office (Excel, Word)

Job description

Parexel is seeking a Clinical Research Associate (CRA) with at least 12 months of onsite monitoring experience to manage clinical sites from initiation through closeout. You will ensure study quality, patient safety, regulatory compliance, and accurate data across multiple therapeutic areas.

You will conduct onsite visits, maintain site relationships, address issues, and support enrollment and study delivery.