Senior CRA II – Ophthalmology/Oncology, Fast-Paced Trials

Fortrea; Pennsylvania; On-site; USD 125,000 - 142,000; Full time

Job summary

Fortrea is seeking Ophthalmology or Oncology Sr. CRAs with 4+ years of monitoring experience to join our Northeast team.

This role focuses on high-quality clinical trial monitoring, site management, and ensuring regulatory compliance across studies. You will travel 30-50% overnight, work in fast-paced environments, and collaborate with cross-functional teams to safeguard data integrity and patient safety in early-phase projects.

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 who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
• Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
• Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
• Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
• Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
• Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
• Assist with training of new employees, eg. co-monitoring
• Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
• Perform other duties as assigned by management

Skills

Clinical Monitoring

Travel readiness

Teamwork

Education

University degree or allied health certification

Job description

Fortrea is seeking Ophthalmology or Oncology Sr. CRAs with 4+ years of monitoring experience to join our Northeast team.

This role focuses on high-quality clinical trial monitoring, site management, and ensuring regulatory compliance across studies. You will travel 30-50% overnight, work in fast-paced environments, and collaborate with cross-functional teams to safeguard data integrity and patient safety in early-phase projects.