- São José do Rio Preto, SP, BR São José do Rio Preto, SP, BR
- De segunda à sexta, das 8h às 17h48 com 1h de almoço
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Professional
•
Tenured - CLT labor code
Description and Responsibilities
The full clinical affairs analyst is a skilled professional who plans, substantiates, builds and conducts a range of clinical affairs activities, including medical writing and ethical/regulatory submissions as required, in territories with similar regulatory systems, for a variety of devices, Partnering with various stakeholders to ensure the successful conduct of clinical investigations targeting different stages of device lifecycles, as well as the appropriateness and sufficiency of clinical data used for product regulatory submissions, while internally ensuring the alignment of technical and operational information with various teams across the company.
Requirements
Minimum requirements:
- Completed bachelor's degree in any relevant field, preferably in biological sciences.
- Minimum of 02 years' experience in Clinical Affairs positions, working with medical devices, or 03 years in similar industries.
- Previous experience in applying Good Clinical Practice in any industry.
Desirable requirements:
- Completed Master's degree or lato sensu postgraduate studies with specialization in relevant subjects.
- Completed doctorate in relevant subjects (can replace up to 01 year of the required experience time).
Benefits
Code: 94169
Registration Date: 2024-10-31
Updated on: 2024-11-11
- Code: 94169
- Registration Date: 2024-10-31
- Updated on: 2024-11-11
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