Senior CRA - Ophthalmology & Oncology (Remote)

Fortrea; Durham (NC); On-site; USD 125,000 - 140,000; Full time

Job summary

Fortrea is seeking a experienced Clinical Monitoring professional to join our team as Local Project Coordinator supporting oncology trials. You will oversee site monitoring, ensure protocol adherence, and maintain data integrity across multiple sites with significant travel.

In this fast-paced, team-oriented role, you will train staff, coordinate projects, and ensure regulatory compliance while delivering high-quality clinical research outcomes.

Qualifications

• 5+ years of Clinical Monitoring experience.
• Oncology experience, early phase preferred.
• Willingness to travel 30–50% overnight.

Responsibilities

• Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties as assigned.
• Responsible for all aspects of site management as prescribed in the project plans
• General On-Site Monitoring
• Ensure the study staff have materials and instructions to safely enter patients into the study
• Ensure informed consent procedures and protocol requirements are adhered to according to regulatory requirements
• Ensure data integrity on CRFs and other data collection tools
• Responsible for registry management and feasibility work as requested
• Complete SAE reporting and follow up of SAEs
• CRF reviews and query resolution per data review guidelines
• Assist with training of new employees (e.g., co-monitoring)
• Coordinate designated clinical projects as Local Project Coordinator
• Perform other duties as assigned by management

Skills

Clinical Monitoring

Oncology experience

Travel readiness

Data management

Regulatory compliance

Education

Bachelor's degree in a related field

Nursing license / allied health certification

Job description

Fortrea is seeking a experienced Clinical Monitoring professional to join our team as Local Project Coordinator supporting oncology trials. You will oversee site monitoring, ensure protocol adherence, and maintain data integrity across multiple sites with significant travel.

In this fast-paced, team-oriented role, you will train staff, coordinate projects, and ensure regulatory compliance while delivering high-quality clinical research outcomes.