Talent Groups
The Pharmacovigilance Scientist will support safety surveillance and signal management activities across clinical and post-marketing products. This role partners closely with PV Physicians and cross-functional teams to manage risk, contribute to regulatory deliverables, and ensure compliance with global pharmacovigilance requirements.
Key Responsibilities
Support product safety surveillance and signal detection activities
Contribute to risk management plans (RMPs/REMS) and benefit-risk assessments
Perform safety data analysis and author safety documentation
Support aggregate reporting (DSURs, PSURs, PADERs)
Provide PV input to clinical and regulatory documents
Collaborate with cross-functional and vendor partners
Qualifications
Life sciences or healthcare degree
2–4 years of pharmacovigilance experience
Experience with safety reporting and MedDRA
Strong communication, analytical, and organizational skills
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Key Responsibilities
Support product safety surveillance and signal detection activities
Contribute to risk management plans (RMPs/REMS) and benefit-risk assessments
Perform safety data analysis and author safety documentation
Support aggregate reporting (DSURs, PSURs, PADERs)
Provide PV input to clinical and regulatory documents
Collaborate with cross-functional and vendor partners
Qualifications
Life sciences or healthcare degree
2–4 years of pharmacovigilance experience
Experience with safety reporting and MedDRA
Strong communication, analytical, and organizational skills
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