Pharmacovigilance Drug Safety Jobs in Bangalore

Novo Nordisk - Bangalore, Karn, IN

meeting requests, packages, and taking meeting minutes. Pharmacovigilance documentation like Drug Safety Update Reports (DSUR), Periodic Safety Update Reports (PSUR), Risk Management Plan (RMP), renewals

from: Novo Nordisk (+1 source) - 21 days ago

Bengaluru, Karnataka, India

information and strategic information) Disclose potential breach of codes or conducts Medical graduation/ M.Pharm / M.Sc/ PhD 6-8 years’ experience in handling Regulatory Affairs and Patient safety

from: jobleads.co.in - 24 days ago

Accenture - Bengaluru

Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance. team handling experience preferred 7+ years of pharmacovigilance experience conducting medical review Not disclosed INR

from: naukri.com - 18 days ago

Accenture - Bengaluru

Please note that this role may require you to work in rotational shifts Qualification Bachelor of Pharmacy Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Not disclosed INR

from: naukri.com - 21 days ago

Teva Pharma - Bengaluru / Bangalore, India

activities within the North American PV unit, in partnership with the Drug Safety Specialists/Pharmacovigilance Safety Specialist and Pharmacovigilance Managers/Director to receive and review adverse event Not Mentioned

from: Monsterindia.com - 5 days ago

Clinilaunch Research Institute Llp - Bengaluru / Bangalore, India

writing and Medical Coding. Ability to perform Quality Control checks and ensure Regulatory Affairs compliance. Knowledge of Pharmacy and experience in drug safety. Excellent attention to detail Not Mentioned

from: Monsterindia.com - More than 30 days ago

GSK India - Bengaluru / Bangalore, India

Pharmaceutical industry experience (eg drug safety (desired), regulatory, clinical development, medical affairs) Working knowledge of key pharmacovigilance regulations and methodologies Good English language Not Mentioned

from: Monsterindia.com - More than 30 days ago

Syneos Health - Bengaluru / Bangalore, India

documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate Not Mentioned

from: Monsterindia.com - 17 days ago