Diverse Lynx · 7 hours ago

Spotfire Technical Lead

United States

Full-time

Remote

Entry Level

1+ years exp

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Computer Software

Growth Opportunities

Hiring Manager

Sunanda K.

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Responsibilities

The Associate pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations.

Qualification

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SpotfirePharmacovigilanceBiomedical literature monitoringAdverse event reportingLife Sciences degreeMedical terminology

Required

Spotfire drug safety

Pharmacovigilance

Master s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.)

At least 1 year of experience reviewing biomedical literature for adverse event reporting OR equivalent combination of education and experience (i.e., an information science degree with at least 1 year of relevant working knowledge of supporting drug and patient safety)

Writing skills to support the creation of succinct, accurate, and precise summaries

Working knowledge of biomedical terminology, drugs, and therapeutic areas