Pharmacovigilance (Pv) (Ra) & Qc

Pharmacovigilance SpecialistJob Description:The role of Pharmacovigilance (PV) Specialist involves managing pharmacovigilance tasks, working under the guidance of the respective Head of Pharmacovigilance. The ideal candidate will have excellent communication and organizational skills, as well as a strong understanding of regulatory requirements in ROW...

Job Title: Pharmacovigilance Associate / Drug Safety AssociateLocation: AmeerpetDepartment: Pharmacovigilance / Drug SafetyReports To: PV Manager / Head of PharmacovigilanceJob Purpose:To ensure patient safety by monitoring, collecting, assessing, and reporting adverse drug reactions (ADRs) and other safety information in compliance with global...

Pharmacovigilance ExpertThe role of a Pharmacovigilance Science Expert is crucial in supporting an international team dedicated to safety surveillance throughout the product lifecycle.This safety expert performs core pharmacovigilance activities, collaborating with Global Safety Leads/Managers to identify, evaluate, and analyze safety data for both marketed...

Company DescriptionDr Reddys Laboratories Ltd is a leading multinational pharmaceutical company based across global locations Each of our 24 000 plus employees comes to work every day for one collective purpose to accelerate access to affordable and innovative medicines because Good Health Cant Wait We started in 1984 with a modest investment 20...

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the...

Company Description Dr. Reddy's Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can't Wait. We started in 1984 with a modest...

**The PV Scientist Manager is responsible for the following**: - Contributes to the planning, preparation, writing and review of non-medical portions of aggregate reports - Works with affiliates and other internal Amgen partners regarding deliverables - Review of AE/SAEs from clinical trials as needed **Contributes under the direction of the Global PV Sr....

Job Summary:We are seeking an experienced Pharmacovigilance Safety professional to lead our ICSRs projects. As a seasoned expert, you will oversee the receipt and processing of adverse event reports, maintain knowledge of client-specific database conventions, and collaborate with internal or external partners for safety database reconciliation.Key...

Role Purpose:The role is responsible for managing Pharmacovigilance Agreements (PVAs) by drafting, reviewing, negotiating, and maintaining them in compliance with business requirements. It ensures accurate records, supports audits, liaises with cross-functional teams, and provides guidance to peers, enabling effective oversight of a large global PVA...

Role Purpose: The role is responsible for managing Pharmacovigilance Agreements (PVAs) by drafting, reviewing, negotiating, and maintaining them in compliance with business requirements. It ensures accurate records, supports audits, liaises with cross-functional teams, and provides guidance to peers, enabling effective oversight of a large global PVA...