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Business intelligence specialist for adverse event reporting

Itabirito
beBeeRegulatory
Eventos
Anunciada dia 4 outubro
Descrição

Job Description

We are seeking a skilled Pharmacovigilance Business Analyst to join our team. As a key member of our organization, you will be responsible for gathering and analyzing requirements for pharmacovigilance systems and workflows.

* Gather and analyze business requirements for pharmacovigilance systems and workflows.
* Collaborate with cross-functional teams, including regulatory, IT, and business users, to implement or enhance safety systems such as Argus, ArisG, and Veeva Vault Safety.
* Document business processes, data flows, and system functionalities related to adverse event reporting.
* Ensure compliance with global regulatory standards.
* Support validation and user acceptance testing of PV systems.
* Provide training and support to end-users on safety systems and processes.
Required Skills and Qualifications
* Bachelor's degree in a relevant field.
* In-depth knowledge of pharmacovigilance processes and regulatory requirements.
* Hands-on experience with safety systems such as Argus, ArisG, and Veeva Vault Safety.
* Familiarity with adverse event reporting workflows and compliance processes.
* Understanding of global pharmacovigilance regulations.
Benefits

This is an exciting opportunity to work with a talented team and contribute to the development of our pharmacovigilance capabilities.

Others

As a Pharmacovigilance Business Analyst, you will have the opportunity to work with cutting-edge technology and make a meaningful impact on the pharmaceutical industry.

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