Remote Oncology Senior CRA II - Fast-Paced Trials

Fortrea; Massachusetts; On-site; USD 125,000 - 140,000; Full time

Job summary

Fortrea is seeking an Oncology Sr. CRA 2 with 5+ years of monitoring experience to oversee clinical sites in the North East US. You will apply clinical judgment and regulatory knowledge to ensure protocol adherence and patient safety in oncology trials.

This role involves on-site and remote coordination, visiting sites, managing CRFs, handling SAE reporting, and traveling 30–50% overnight to study sites. A university degree or related certification is required.

Qualifications

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

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 the proper materials and instructions to safely enter patients into the study.
• Ensure patient protection by verifying informed consent procedures and protocol requirements.
• Ensure data integrity on CRFs and other data collection tools; monitor for missing or implausible data.
• Responsible for registry management as prescribed; undertake feasibility work when requested.
• Complete SAE reporting and follow-up of SAEs.
• Independently perform CRF review; query generation and resolution.
• Assist with training of new employees, e.g., co-monitoring.
• Coordinate designated clinical projects as Local Project Coordinator and act as local client contact as assigned.
• Perform other duties as assigned by management.

Skills

Clinical monitoring

Oncology experience

Education

University degree or allied health certification

Job description

Fortrea is seeking an Oncology Sr. CRA 2 with 5+ years of monitoring experience to oversee clinical sites in the North East US. You will apply clinical judgment and regulatory knowledge to ensure protocol adherence and patient safety in oncology trials.

This role involves on-site and remote coordination, visiting sites, managing CRFs, handling SAE reporting, and traveling 30–50% overnight to study sites. A university degree or related certification is required.