Clinical Trials Assistant - Exclusive for PWD

IQVIA; São Paulo; Híbrido; BRL 20.000 - 80.000; Tempo integral

Resumo da oferta

A leading clinical research services provider in São Paulo is seeking an experienced administrative support professional. The role involves assisting with the maintenance of clinical documentation, tracking Case Report Forms, and supporting Clinical Research Associates. Ideal candidates will have a Bachelor's Degree in Life Sciences and at least 1 year of experience in a healthcare setting. This is a hybrid position based in São Paulo.

Qualificações

• 1 year of experience in a healthcare environment or equivalent.
• Experience in contract negotiation or start-up activities is preferred.
• Upper-intermediate English skills are required.

Responsabilidades

• Assist with updating and maintaining clinical documents for projects.
• Prepare, handle, and archive clinical documentation and reports.
• Track Case Report Forms and manage clinical data flow.

Conhecimentos

Clinical document management

Administrative support

Communication

Time management

Formação académica

Bachelor’s Degree in Life Sciences

Descrição da oferta de emprego

Overview

Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.

Essential Functions

• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
• Assist with periodic review of study files for completeness.
• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.

Qualifications

• Bachelor’s Degree Life sciences ideally.
• Ideally 1 years’ experience in a healthcare environment or equivalent combination of education, training and experience, with experience in contract negotiation (CTA amendment negotiation) or start up activities. Other administrative experience is highly valuated.
• Upper-intermediate level of English.

Hybrid role: offices are in Sao Paulo, SP.

Please submit your CV and laudo when applying.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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