FSP Clinical Research Associate 2 - Las Vegas, NV - Oncology

Fortrea•Durham, NV

13d•$100,000 - $112,000•Hybrid

About The Position

The FSP Clinical Research Associate 2 monitors and manages clinical trial sites, with a focus on oncology studies. The role involves 8–10 days on site per month, combining onsite and remote work, and requires candidates in the Las Vegas, Nevada area. It includes frequent travel, with 60% overnight travel expected. The CRA provides a high standard of care for clinical trial participants and responds to emergency situations in accordance with clinical research standards. The position works in a fast-paced, changing, team-oriented, technology-based environment where protocol adherence and timely execution are essential. Work is primarily performed in an office environment, with frequent travel to client and site locations and occasional domestic and international travel.

Requirements

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (for example, nursing licensure).
Two years of clinical monitoring experience.
60% overnight travel.
Oncology experience.
Comfort working in a fast-paced environment with strict protocol and timeline requirements, changing priorities, and a technology-based data-collection environment.
Teamwork and people skills.

Responsibilities

Conduct all aspects of study site monitoring, including routine monitoring, site close-out, study-file maintenance, pre-study visits, and initiation visits.
Manage sites as prescribed in project plans and conduct general onsite monitoring.
Liaise with vendors and undertake feasibility work when requested.
Ensure study staff receive the appropriate materials and instructions to safely enroll patients in the study.
Verify that informed-consent procedures and protocol requirements are followed in accordance with applicable regulatory requirements to protect study participants.
Verify the integrity of data submitted on Case Report Forms (CRFs) and other data-collection tools through careful source-document review, and monitor for missing or implausible data.
Manage registries as prescribed in project plans.
Complete Serious Adverse Event (SAE) reporting, prepare reports and narratives, and follow up on SAEs.
Independently review CRFs and generate and resolve queries using established data-review guidelines on Fortrea or client data-management systems, as assigned by management.
Assist with training new employees, including co-monitoring.
Coordinate designated clinical projects as a Local Project Coordinator, with supervision if applicable, and act as a local client contact when assigned.
Perform other duties as assigned by management.