Study Start Up Associate

2 semanas atrás

Sao Paulo, Brasil Docs Global Tempo inteiro

SSU responsibilities:

- Coordinate guide and assist with all start up activities prior to site activation, including but not limited to:

- Site Informed Consent Form (ICF) localization and guidance in line with regulatory/health authority requirements.
- Ethics Committee information, meeting dates & costs.
- Ethics & Governance submission processes.
- Contracts & Indemnity request process.
- For global studies, localize global Informed Consent Form (ICF) with country requirements.

What is Required
Proven external/independent clinical trial assistance experience gained in the country
Life science degree (BSc) o RN (registered nursing qualification)

Full working eligibility
Able to work effectively within fast-paced working environments

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

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