CRA II: Oncology Monitoring & Site Leadership

PSI CRO

Seattle (WA)

Presencial

USD 85.000 - 110.000

Jornada completa

14 días+

Generador de candidaturas

Una candidatura hecha a medida para este puesto de trabajo — un currículum y una carta de presentación adaptados que responden directamente a la oferta.

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Descripción de la vacante

PSI CRO is seeking an experienced Clinical Research Associate to monitor multicenter clinical trials. This role involves onsite monitoring visits, site management, data verification, and collaboration with sponsors and sites on study conduct.

A strong background in oncology is preferred, with travel up to 75% across sites on the West Coast region. Qualified candidates will have a Life Sciences degree, 2+ years on-site monitoring experience, and proficiency in English and MS Office.

Formación

Bachelor’s degree in Life Sciences or equivalent.
Located on the West Coast region preferred.
2+ years of independent on-site monitoring experience.
Experience in Oncology mandatory; GI or radio-pharm experience preferred.
Full working proficiency in English.
Proficiency in MS Office applications.
Ability to travel up to 75%.
Valid driver’s license (if applicable).

Responsabilidades

Act as the main line of communication between the project team, sponsor, and the site.
Build and maintain a good relationship with the site staff involved in the study conduct.
Prepare, conduct, and report site initiation, routine monitoring and close-out visits.
Ensure recruitment targets are defined, communicated, recorded and met, and timelines are followed at site level.
Ensure timely information flow with trial sites on Adverse Events and protocol deviations.
Perform source data verification and follow up on data queries at site level.
Review ISF/TMF at site level and ensure study documents are reconciled.
Conduct site audits and resolve audit findings as needed.
Support regulatory submissions and site readiness activities.