Senior CRA — Home-Based (West Coast Travel)

Worldwide Clinical Trials; Sacramento (CA); Remote; USD 95,000 - 150,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee high-quality clinical studies across investigative sites on the West Coast. You will lead site qualification, monitor visits, and ensure protocol adherence and regulatory compliance, traveling ~8–10 days monthly while maintaining strong sponsor and site relationships.

The role is home-based, require 5+ years of regional CRA experience, and emphasis on Oncology trials with hematology exposure.

Qualifications

• Bachelor's Degree or Nursing Degree plus 5+ years as a regional traveling CRA.
• Experience monitoring Oncology clinical trials; Hematology experience preferred.
• Requires travel within the specified region; travel 8–10 days per month.
• Strong knowledge of clinical trial processes, site management, and regulatory requirements.

Responsibilities

• Manage clinical research activities at investigative sites participating in Worldwide clinical studies.
• Coordinate study start-up activities, including collection of regulatory documentation and support of contract and budget processes.
• Conduct all types of monitoring visits: PSSVs, SIVs, IMVs and COVs.
• Train site personnel on protocol requirements, data collection processes, and safety reporting expectations.
• Monitor site performance and provide ongoing support throughout study maintenance activities.
• Ensure compliance with informed consent requirements, safety reporting obligations, and applicable regulatory standards.
• Partner with sites and study teams to drive data quality, participant safety, and overall study success.
• Support site closeout activities and ensure study requirements are completed at the conclusion of the trial.

Skills

Oncology monitoring experience

Full-service monitoring experience

Regional traveling CRA experience

Regulatory knowledge

Site management

Education

Bachelor's Degree or Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee high-quality clinical studies across investigative sites on the West Coast. You will lead site qualification, monitor visits, and ensure protocol adherence and regulatory compliance, traveling ~8–10 days monthly while maintaining strong sponsor and site relationships.

The role is home-based, require 5+ years of regional CRA experience, and emphasis on Oncology trials with hematology exposure.