Remote Clinical Research Associate - Site Monitoring

Parexel; Salem (OR); On-site; USD 70,000 - 100,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate (CRA) to manage investigator sites, monitor trials from activation to close-out, and ensure patient safety and quality. You will work with a cross-functional study team, coordinate with the Site Care Partner, and travel extensively to sites (60–80%).

A life sciences degree and English fluency are required. Responsibilities include coordinating enrollment, maintaining regulatory compliance, and supporting data integrity throughout the study

Qualifications

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations.
• Monitoring Experience: Minimum 2 years relevant experience in clinical research site monitoring.
• Must be fluent in English and in the native language(s) of the country they will work in.
• Ability to travel 60-80%.
• Valid driver's license and passport required.

Responsibilities

• Ensure proper conduct of clinical trials in accordance with the SMP, laws, GCP, and sponsor standards to achieve project goals, timelines and quality.
• Manage site activation through database lock, ensuring timelines and quality deliverables are met.
• Serve as the primary contact for investigator sites; coordinate with SCP to ensure site delivery quality.
• Interface with the study team, vendors, and investigator sites to facilitate information flow.
• Perform investigator site development, coaching and training to ensure protocol compliance and patient safety.
• Attend investigator meetings and support enrollment; assist with recruitment initiatives at site level.
• Conduct onsite, remote/electronic monitoring per SMP and SOPs.
• Monitor AEs/SAEs and collaborate with Drug Safety; follow up to resolution.
• Submit required reports and TMF documentation within deadlines.
• Identify and resolve site issues; implement corrective actions and CAPAs.
• Resolve data queries; prepare site close-out plans and conduct close-out activities.
• Ensure oversight of investigational product at the site, including handling and storage.
• Support database release as needed.
• May undertake unblinded monitoring responsibilities.

Skills

Clinical trial knowledge

Monitoring experience

Fluency in English

Travel flexibility

Valid driver's license & passport

Education

Bachelor's in life sciences or related field

Job description

Parexel is seeking a Clinical Research Associate (CRA) to manage investigator sites, monitor trials from activation to close-out, and ensure patient safety and quality. You will work with a cross-functional study team, coordinate with the Site Care Partner, and travel extensively to sites (60–80%).

A life sciences degree and English fluency are required. Responsibilities include coordinating enrollment, maintaining regulatory compliance, and supporting data integrity throughout the study