Pharmacovigilance Data Specialist – Adverse Event Management
Pfizer
Parsippany-Troy Hills (NJ)
On-site
USD 48,216 - 55,104
Full time
14 days+
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Benefits offered by this job
Comprehensive Benefits Package
Short-Term Disability
Long-Term Disability
Life Insurance
Job summary
A leading pharmaceutical company in Parsippany-Troy Hills is seeking a Safety Data Management Specialist. This role involves reviewing and processing reports of adverse drug experiences to ensure regulatory compliance. Candidates should have a Bachelor's degree in a science discipline and experience in pharmacovigilance is preferred. The position offers a pay rate of $35-$40 per hour. Join our dynamic team where you will contribute to drug safety initiatives and work closely with various stakeholders.
Qualifications
Health Care Professional or equivalent experience preferred.
Ability to solve routine problems with supervision.
Fluency in spoken and written English.
Responsibilities
Carry out case processing activities.
Review and document case-related information.
Assess and process cases based on criteria.
Skills
Experience in pharmacovigilance
Medical writing skills
Computer literacy
Experience with relational databases
Education
Bachelor's degree in science discipline
Job description
A leading pharmaceutical company in Parsippany-Troy Hills is seeking a Safety Data Management Specialist. This role involves reviewing and processing reports of adverse drug experiences to ensure regulatory compliance. Candidates should have a Bachelor's degree in a science discipline and experience in pharmacovigilance is preferred. The position offers a pay rate of $35-$40 per hour. Join our dynamic team where you will contribute to drug safety initiatives and work closely with various stakeholders.