Senior CRA II - Medical Device Trials, Travel-Heavy

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

Job summary

Fortrea is seeking a Senior CRA II for Central-based field monitoring with 1+ year of device experience and 3+ years of monitoring background. This role involves leading site monitoring, site management, and ensuring adherence to regulatory guidelines.

Expect travel 60-80% and responsibilities spanning protocol development, data integrity, and coordination with sponsors and vendors. The ideal candidate holds a life sciences degree, fluent English, and the ability to work independently in a

Qualifications

• Requires a university or college degree in life sciences or related field.
• Thorough understanding of regulatory requirements and drug development process.
• Fluent in English; able to work in a global regulatory environment.

Responsibilities

• Monitor study sites and manage site monitoring activities, including routine monitoring and closeout.
• Ensure proper informed consent procedures and protocol adherence.
• Prepare trip reports and manage project tasks under supervision.
• Coordinate with investigators, vendors, and trial management to ensure timelines.
• Assist with protocol development, CRF reviews, and data quality reviews.

Skills

Clinical monitoring

SAE reporting

Line management

Communication

Education

Bachelor's degree in life sciences

Job description

Fortrea is seeking a Senior CRA II for Central-based field monitoring with 1+ year of device experience and 3+ years of monitoring background. This role involves leading site monitoring, site management, and ensuring adherence to regulatory guidelines.

Expect travel 60-80% and responsibilities spanning protocol development, data integrity, and coordination with sponsors and vendors. The ideal candidate holds a life sciences degree, fluent English, and the ability to work independently in a