Senior Clinical Research Associate – Remote Monitoring

Parexel; Boise (ID); Remote; USD 90,000 - 120,000; Full time

Job summary

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to oversee site management, monitoring, and close-out for assigned clinical trials.

You will ensure patient safety, regulatory compliance, and high-quality execution across sites, working closely with the Site Care Partner and study team. The role requires extensive knowledge of GCP/ICH, FDA regulations, and hands-on monitoring experience, with travel up to 60-80%.

Qualifications

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations.
• Monitoring experience: minimum 2 years in clinical research site monitoring.
• Must be fluent in English and in the country language where you work.

Responsibilities

• Ensure proper conduct of clinical trials per SMP, laws, GCP and sponsor standards.
• Manage site activation through database lock with on-time, quality deliverables.
• Serve as primary contact for assigned investigator sites and coordinate with SCP.
• Interface with study team, vendors, and sites to ensure efficient information flow.
• Develop investigator site training and address protocol questions from site staff.
• Attend investigator meetings and support enrollment and recruitment initiatives.
• Conduct onsite/remote monitoring and close-out activities per SOPs.
• Monitor AE/SAE with Drug Safety Unit and ensure timely SAE resolution.
• Submit all TMF and site documentation within required timeframes.
• Identify and resolve investigator site issues and implement CAPAs.
• Oversee investigational product handling at sites (receipt, storage, destruction).
• Support database release as needed.
• May perform unblinded monitoring when appropriate.

Skills

Clinical trial methodologies, ICH/GCP

FDA regulations

Investigator site monitoring

English fluent

Travel 60-80%

Driver’s license & passport

Education

Bachelor’s degree in life sciences or related field

Job description

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to oversee site management, monitoring, and close-out for assigned clinical trials.

You will ensure patient safety, regulatory compliance, and high-quality execution across sites, working closely with the Site Care Partner and study team. The role requires extensive knowledge of GCP/ICH, FDA regulations, and hands-on monitoring experience, with travel up to 60-80%.