Drug Safety Jobs in Mumbai
Integrated Personnel Services Limited - Mumbai Metropolitan Region
drugs and drugs in development through periodic medical review training held by client medical staff. Skills required: • Computer Literate (good knowledge of MS Office) • Sound understanding of the Drug
from: linkedin.com - 7 days ago
Astellas Pharma - Mumbai, Maharashtra, India
Purpose & Scope: Pharmacovigilance (50%) In coordination with the PV Affiliate Lead/Drug Safety Officer (DSO): This function is responsible for maintenance of excellence in Pharmacovigilance (PV
from: linkedin.com - 5 days ago
Fortrea - Mumbai
, Periodic Adverse Drug Experience Reports, Periodic Benefit-Risk Evaluation Reports, Development Safety Update Report, ACOs, Addendum reports, as assigned. Author and review RMPs, adhoc reports, Benefit-Risk Not disclosed INR
from: naukri.com - 12 days ago
Unichem Laboratories Limited - Mumbai, Maharashtra, India
of drug safety regulatory requirements. Ability to coordinate with internal and external stakeholders. Excellent communication and presentation skills Experience in PSURs, PBRERs report writing. Knowledge
from: linkedin.com (+1 source) - 22 days ago
Mumbai, India
We are seeking a full-time Clinical Safety Coordinator to join our team in India. This role focuses on handling adverse events from various sources, including clinical trials and post-marketing surveillance... Not Mentioned
from: Monsterindia.com - 10 days ago
Mumbai, Navi Mumbai
Research (drug safety) preferred. Salary up-to 20LPA Roles & Responsibilities: • Accountable for the medical review of relevant clinical, other solicited and spontaneous cases (including literature articles 100000-1800000
from: Monsterindia.com - 5 days ago
Mumbai, India
for adverse drug reactions and serious adverse events. Quality Control: Perform quality reviews of safety reports prepared by junior or associate medical writers. Document Development: Develop strategies Not Mentioned
from: Monsterindia.com - 3 days ago
Mumbai, India
development for new and existing drug products, manage projects, and author technical documents. The role needs to comply with safety and regulatory requirements, communicate testing status, and perform Not Mentioned
from: Monsterindia.com - 4 days ago
Navi Mumbai, Mumbai, India
This role involves handling and processing adverse events from various sources, including clinical trials and post-marketing surveillance. This position offers an exciting opportunity for individuals with... Not Mentioned
from: Monsterindia.com - 3 days ago
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