Job Description:
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* Act as a key liaison between business stakeholders, regulatory teams, and IT to ensure accurate and compliant adverse event reporting.
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Responsibilities:
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* Safety Systems Implementation
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* Regulatory Compliance Evaluation
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* Business Process Documentation
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Requirements:
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* Bachelor's degree in Life Sciences, Pharmacy, or IT.
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* In-depth knowledge of pharmacovigilance processes and regulations.
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* Experience working with safety systems such as Argus, ArisG, and Veeva Vault Safety.
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Familiarity:
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* Pharmacovigilance regulations.
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* Adverse event reporting workflows.
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* Documentation and reporting tools.
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Certifications:
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* Certification in pharmacovigilance is highly desirable but not mandatory.
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