FSP - CRA - Oncology - West Coast

FSP - CRA 2 - Oncology - West Coast

Join to apply for the FSP - CRA 2 - Oncology - West Coast role at Fortrea
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Our FSP team is currently seeking CRA 2s with 1+ year of monitoring and strong Oncology monitoring experience, residing within one hour of a major airport in California, Nevada, Washington, Idaho, New Mexico, Colorado, Arizona or Utah. This role will have regionalized travel around 30%+.

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

• 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 monitoring, 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 reports, 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, e.g., 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.

• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).
• 1‑3+ years of Clinical Monitoring experience.
• Oncology experience is required.
• West Coast location.
• 30‑40% overnight travel.

Regular, full‑time or part‑time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:

• Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers).
• 401(K).
• Paid time off (PTO) – Flex Plan.
• Employee recognition awards.
• Multiple ERG’s (employee resource groups).
• Target Pay Range (based on title): $105‑114K.

• Work is performed in an office environment with exposure to electrical office equipment.
• Frequent travel to clients/site locations with occasional travel both domestic and international.

• Ability to sit for extended periods and operate a vehicle safely.
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
• Ability to access and use a variety of computer software developed both in‑house and off‑the‑shelf.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15‑20 lbs.
• Regular and consistent attendance.
• Varied hours may be required.

Remote

Applications will be accepted on an ongoing basis.

Learn more about our EEO & Accommodations request here.