- Pharmacovigilance / Drug Safety Trainees/Interns openings in Bangalore - Freshers and Experienced
1.Drug Safety / Pharmacovigilance Trainee/Interns (10) - Freshers-Any year of passing out. Location:Bangalore
You would be placed in the Pharmacovigilance Department as a Pharmacovigilance/Drug Safety Associate after the successful completion of the traineeship period in the Organisation.
Eligibility: (Any year of passing out)
- Bachelors/Masters in LifeSciences (Microbiology, Biotechnology, Biomedical, Biochemistry, Pharmacology, Anatomy, Immunology, Parasitology, Genetics etc) B.Sc/Msc Nursing, BDS, BHMS,BAMS ,B.Pharm, Mpharm,MBBS,Veterinary Science,B.Tech etc
-Excellent oral and written communication skills
-Willing to undergo In-house Traineeship/Internship
-Willing to relocate to Bangalore
Successful Trainee/Interns will be promoted as Drug Safety Associates in our Organisation.
Email your CV to: hr@tpmet.com,
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
Eligibility criteria:
- 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 skillset
- Willing to travel to Europe and adapt to new business environment quickly
-Willing to undergo In-house Internship
Email your CV to: hr@tpmet.com,
career@tpmet.com
Ph: +91-7406777808
080-65777808
080-65777808
Desired Candidate Profile
Education-
- Please refer to the Job description above
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