Clinical Research Associate

Act as the
Siga leyendo para descubrir lo que necesitará para tener éxito en este puesto, incluyendo habilidades, cualificaciones y experiencia.
main point of contact
and support for the assigned investigational sites.
Prepare, conduct, and report
remote and onsite monitoring visits
in accordance with the Monitoring Plan and applicable SOPs.
Assess investigational site performance and ensure
compliance with study protocol, GCP, and regulatory requirements .
Perform all required activities during monitoring visits according to internal and/or sponsor procedures.
Document and track the
management of issues and deviations
identified during and between site visits.
Support investigational site staff in the
resolution of issues/deviations
and the development of
Corrective and Preventive Action (CAPA) plans .
Collaborate with
Biometry, Regulatory Affairs, and Safety
departments to obtain necessary ...