CRA II: Clinical Monitoring & Site Leadership

Linical; United States; Hybrid; USD 95,000 - 135,000; Full time

Benefits offered by this job

PTO

Comprehensive benefits

Job summary

Linical is seeking a Clinical Research Associate II to support West Coast USA trials. You will monitor sites, manage visit schedules, and help ensure data quality and regulatory compliance across complex studies.

Ideal candidates hold a life sciences degree or nursing background, CRA training, and are willing to travel up to 75%. Strong communication and organizational skills are essential to collaborate with study teams and vendors in a global CRO environment.

Qualifications

• Life Science degree or nursing background, or equivalent education/experience with CRA training.
• Proven monitoring and site management experience in clinical studies.
• Strong knowledge of clinical research processes, GCP, and applicable regulations.
• Excellent communication, organization, and problem-solving skills.
• Willing to travel up to 75% and hold a valid driver’s license.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits for complex studies.
• Ensure safety and well-being of participants by overseeing site compliance with clinical protocols, regulations, and GCP.
• Perform source data verification and drive data quality through documentation.
• Collect regulatory documents and train site personnel on study requirements.
• Support submissions to ethics committees and regulatory authorities.
• Maintain Trial Master File (TMF), facilitate site payments, and manage visit scheduling.

Skills

CRA monitoring & site management

GCP knowledge

Regulatory knowledge

Communication

Travel readiness

Driver's license

Education

Life Science degree / nursing background / equivalent education

Job description

Linical is seeking a Clinical Research Associate II to support West Coast USA trials. You will monitor sites, manage visit schedules, and help ensure data quality and regulatory compliance across complex studies.

Ideal candidates hold a life sciences degree or nursing background, CRA training, and are willing to travel up to 75%. Strong communication and organizational skills are essential to collaborate with study teams and vendors in a global CRO environment.