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| Job Location | Bangalore |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Medical / Healthcare |
| Functional Area | Sales / BD |
| EmploymentType | Full-time |
1. Drug Safety / Pharmacovigilance Associates(10) - Freshers- Any year of passing out. Selected candidates would be placed in Terzetto Pharma Metrics as a pharmacovigilance / Drug Safety Associate after the successful completion of the Pharmacovigilance Traineeship. Bachelors / Masters in Lifesciences (Microbiology, Biotechnology, Biomedical, Biochemistry, Pharmacology, Anatomy, Immunology, Parasitology, Genetics etc) B. Sc/ Msc Nursing, BDS, BHMS, BAMS , B. Pharm, M. Pharm, MBBS, Veterinary Science, B. Tech etc Must have excellent oral and written communication skills Selected candidates would undergo In- house Traineeship Must be willing to relocate to Bangalore Please email your resume in word format and send to career@tpmet. com 2. Pharmacovigilance Officer Positions (5) - Min experience 3 years. Location : Bangalore Bachelors/ Masters in Lifesciences (Microbiology, Biotechnology, Biomedical, Biochemistry, Pharmacology, Anatomy, Immunology, Parasitology, Genetics etc) B. Sc Nursing, BDS, BHMS, BAMS , B. Pharm, Mpharm, , MBBS, B. Tech etc An ideal candidate will be a complete team player, focused on AE reporting and outsourced case processing ability and strict ability to meet the timelines. Role : Processing of adverse events reports originating different region and source. Project Monitor and manage the client relation for PVG . Additional responsibility to be a contact to the client in absence of Team lead . Make sure all the process are as per SOP and timelines. Case processing, triage and narration writing skills Involve in preparation for audits/ inspections. Should have strong knowledge of EU vigilance systems. Should have a valid passport to travel Europe Master Degree in Pharmacy or Lifesciences or equivalent with a minimum of 3 years of experience Strong Pharmacovigilance experience within a Pharmaceutical company or CRO. Strong Case processing experience, ideally both with clinical and post- approval adverse events. Strong understanding of Pharmacovigilance process and standard working procedures. Excellent English communication skills both written and verbal. Fully aware of current Pharmacovigilance regulations and legislation. Project Management skills; good organisational, planning, co- ordination, follow up skills. Strong software learning skills, and willing to update skill set Willing to travel to Europe and adapt to new business environment quickly,
Keyskills :
drug safetynew businesslife scienceswriting skillsadverse eventsborder controlcase processingmanagement skillsproject managementcommunication skillswritten communicationclient relationcomsop