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Há 11 horas
**Job Title:** Pharmacovigilance Associate
Description:This role involves reviewing and processing safety events, abstracts, and full articles to identify safety information from literature sources. You will also be responsible for generating data listings from the safety database and ensuring accuracy of the data.
Responsibilities:- Review and process premarketing, post-marketing, medical device, and drug safety events and other medically related information.
- Perform review of abstracts and full articles to identify safety information from literature sources.
- Generate data listings from the safety database and ensure accuracy of the data.
- Provide input and review relevant safety tracking systems for accuracy and quality.
- Attend project team meetings and teleconferences as required.
- Bachelor Degree in health sciences.
- Experience supporting safety intake, assessment, and report to regulatory entities.
- Knowledge of company policies and procedures, computerized information systems, standard application software, and working in safety databases.
- Advanced English.
- A range of benefits to support your well-being and work-life balance.
- An inclusive and accessible environment for all candidates.
- A commitment to providing a workplace free of discrimination and harassment.
We are looking for a highly skilled and detail-oriented individual to join our team. If you have a strong background in pharmacovigilance and excellent communication skills, we encourage you to apply for this exciting opportunity.
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