Onsite CRA: Clinical Site Monitoring Pro

Parexel; Salem (OR); On-site; USD 75,000 - 105,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending & Health Savings

Work/Life Balance

401(k) with Company match

Pet Insurance

Job summary

Parexel in the United States is seeking a Clinical Research Associate (CRA) with at least 12 months of onsite monitoring experience to join our team in Oregon. You will manage clinical sites from qualification through closeout, ensuring study quality, patient safety, regulatory compliance, and data integrity.

You will conduct site monitoring visits, build strong site relationships, support enrollment, and help deliver study milestones.

Qualifications

• Onsite CRA monitoring experience of 12+ months.
• Bachelor’s degree in biological science, pharmacy, or health-related discipline.
• Knowledge of GCP, regulatory requirements, and clinical trial processes.
• Experience with CTMS, EDMS, and MS Office applications (Excel, Word).
• Strong interpersonal, written, verbal, organizational, and problem-solving skills.
• Oncology, Ophthalmology, CAR-T, and/or MASH trial monitoring experience preferred.

Responsibilities

• Conduct qualification visits, SIV, MV, and TV with timely reports.
• Manage site quality and delivery from identification to closeout.
• Serve as primary site contact to address questions and resolve issues.
• Oversee study integrity and relationships with investigators and staff.
• Review trial performance and safeguard participant safety.
• Develop patient recruitment strategies with sites.
• Ensure compliance with SOPs, protocols, GCP and regulatory requirements.
• Evaluate data quality and site performance; verify documentation.
• Monitor regulatory documentation completeness and site file verification.

Skills

Site relationship management

Communication skills

Independent work

Problem solving

Prioritization

Team collaboration

Education

Bachelor’s degree in biological sciences

Tools

CTMS

EDMS

MS Office (Excel/Word)

Job description

Parexel in the United States is seeking a Clinical Research Associate (CRA) with at least 12 months of onsite monitoring experience to join our team in Oregon. You will manage clinical sites from qualification through closeout, ensuring study quality, patient safety, regulatory compliance, and data integrity.

You will conduct site monitoring visits, build strong site relationships, support enrollment, and help deliver study milestones.