Senior CRA II - Medical Device Trials Lead

Fortrea; California; On-site; USD 130,000 - 133,000; Full time

Job summary

Fortrea's FSP team is seeking an experienced Central based Senior CRA with 3+ years monitoring experience and device knowledge. The Senior CRA II will oversee site monitoring, site management, and lead projects with local coordination responsibilities.

Travel 60-80% overnight, including domestic and international sites, is expected. Candidates should be fluent in English, understand regulatory requirements, and operate under Fortrea SOPs.

Qualifications

• Bachelor’s degree or higher in life sciences or related field.
• Regulatory requirements understanding across countries.
• Knowledge of the drug development process.
• Fluent in English (written and spoken).
• Relevant experience may substitute for degree.

Responsibilities

• Monitor clinical sites, perform routine monitoring and closeouts.
• Manage site communications, visit planning, and vendor liaising.
• Ensure informed consent and protocol adherence per regulations.
• Maintain CRFs and data integrity through source document review.
• Coordinate monitoring plans and trip report reviews.
• Lead small projects and act as local project coordinator when assigned.
• Train and mentor junior staff; assist with protocol development.

Skills

Clinical Monitoring

Site Monitoring

Study Site Management

Registry Administration

Driver's License

Education

Life Science degree

Allied Health Certification

Job description

Fortrea's FSP team is seeking an experienced Central based Senior CRA with 3+ years monitoring experience and device knowledge. The Senior CRA II will oversee site monitoring, site management, and lead projects with local coordination responsibilities.

Travel 60-80% overnight, including domestic and international sites, is expected. Candidates should be fluent in English, understand regulatory requirements, and operate under Fortrea SOPs.