
Safety Data Specialist in Dublin
24 hours ago
This position involves the detection, assessment, and evaluation of signals in pharmacovigilance. It requires a deep understanding of safety data and the ability to communicate effectively with stakeholders.
The successful candidate will be responsible for:
- Conducting signal detection activities as per the defined schedule and documenting all outputs produced.
- Reviewing and assessing potential signals/new safety concerns and coordinating/documenting resulting actions with relevant stakeholders.
- Maintaining up-to-date status of all risk management plans (RMPs) and managing Regulatory Affairs' requests related to RMPs updates/submissions.
- Degree in life sciences.
- Minimum 5 years of experience in safety/pharmacovigilance in biotech, pharma, or clinical research organization.
- Strong working knowledge of PV global regulations and guidelines with PV operational knowledge.
This is an exciting opportunity for professionals interested in advancing their careers in pharmacovigilance. The role offers a chance to work with a dynamic team, contribute to the development of safety strategies, and make a meaningful impact on patient safety.
How to Apply:If you are interested in this opportunity, please submit your CV to the designated contact person. We look forward to hearing from you.
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