Teva Pharmaceuticals Jobs Opening Details |
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Job in Pharmacovigilance Associate at Teva Pharmaceuticals
Teva Pharmaceuticals Pharmacovigilance Associate Job openings in Bangalore location. Interested and eligible Candidates Apply Now
Company: Teva Pharmaceuticals
Job Description
Data collection/generation, authoring, and preparation of selected PSUR sections,
Review/QC of selected PSUR sections,
PSUR finalization (creation of PSUR pdf),
Drafting responses to requests from regulatory agencies, as required,
Making sure assigned PSUR-related activities are performed in line with working procedures,
Collaborative working relationships with other functions in Teva,
Any other task assigned by the direct manager
Working experience with databases (e.g. ARIGg, Argus, Cognos, Veeva, TrackWise, QlikSense)
Minimum 2 years of experience in Pharmacovigilance (PSUR/RMP/PADER writing, or ISCR/case processing)
Excellent organizational skills
Strong sense for compliance and deadlines
Qualifications
University degree (bioscience background)
Active knowledge of English, both written and spoken
MS Office skills (Word, Excel, PowerPoint)
Function: Regulatory Affairs
Sub Function: Pharmacovigilance
Teva Pharmacovigilance Associate Job Information :
Pharmacovigilance Associates (I & II)
Job Location: Bangalore
Experience: Minimum 2 years of Pharmacovigilance experience, ICSR/case
processing & related activities.
Qualification: Post graduates in Science or Pharmacy/HCPs.
PV Associates I
Processing adverse events report into Teva’s global safety database.
The different sources/types of reports include Reports from the scientific literature.
Teva partners (other pharmaceutical companies). Health authorities studies & other programs.
The processing includes Adverse events coding (in medical dictionary-MedDRA), drug coding in the company product dictionary & WHO DD seriousness, and labeling assessment & submission to health authorities.
PV Associates II
ICSR processing
Conducting quality checks for ICSRS Participate in fact as an expert in PV data management including ICSR collection & exchange, processing, and assessment, distribution & submission, quality & compliance monitoring for ICSRS & end-to-end overview on these activities
Application Process: Teva brings an opportunity for Pharmacovigilance professionals in our Risk management division. Please share your cv with the subject line RMP in my email address – poulomi.mitra@teva.co.in
Location – Bangalore
Experience range – 2-3 yrs any exposure in PV Please mention your current CTC while applying. This is a global opportunity and people who have worked for global clients or stakeholders will have an advantage.
Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment.
It is Teva’s global policy that equal employment opportunities be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable law