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Pharmacovigilance Associate

Omasy Research
Experience : 0 to 3 Years
Education : M.Pham, MBBS, BSc, MDS, BE/B.Tech, MSc, B.Pharm, BDS
Location : Bangalore
Job Role : Others
Posted on 08 Oct 20
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Job DescriptionLast Date 07 Dec 20

Exp: 0 to 1 Years,

Pharmacovigilance Associate- FRESHERS(2019-20 can also Apply)

Job Summary
  • As a Pharmacovigilance Associate / Drug Safety Officer you will support the Pharmacovigilance Department (or Drug Safety Department) in fulfilling the obligations for reporting side effects within the current Dutch and European legislation for pharmacovigilance / drug safety You will also train colleagues in the marketing and sales departments, as well as medical and clinical departments on compliance with their reporting responsibilities for Drug Safety Furthermore you will communicate with your companies headquarters on PV/DS matters, both spontaneous marketed drug related (unsolicited) AE’s and SAE’s but also clinical study related events One of the fundamental principles of reporting adverse events is determining what an Individual Case Safety Report (ICSR) is During the triage-phase of a report on possible side effects, it is important to determine whether the “four elements” of a valid ICSR are present: (1) an identifiable patient, (2) an identifiable reporter, (3) a drug, and (4) a side effect Synonyms for the Pharmacovigilance Associate (PVA) are Drug Safety Officer (DSO) and Patient Safety Specialist
  • Job Location: Bangalore/ Hyderbad/ Pune (Direct/ Work from home options available)

Required Candidate profile:

Only Freshers are eligible- Bsc, MSc Life Sciences, BPharma, MPharma, Pharm D, BDS,BHMS,BAMS,BUMS,BDS,MDS,MBBS,BTech Biotechnology, Biomedicals, Microbioloy

  • Pharmacovigilance Associate
  • Experience : 0 to 3
  • Job Type : Full Time
  • Interview Type : Face to Face Interview


Job Type : Full Time
Interview Type : Face to Face Interview
Company Description
Omasy Research
Apply now
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