Pharmacovigilance Associate

Who we areTogether, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic...

Who we are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic...

Who we areTogether, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic...

The opportunity The Global PV Clinical Operations team member ensures case processing for safety information from pre-authorization studies is in line with regulatory requirements, best practices, and Teva internal procedures. Contributes to operational aspects of pre-authorization studies for Teva products worldwide, aiming to simplify processes and ensure...

About the Role of Drug Safety Associate at GSS Pharma Pvt.LtdGSS Pharma Pvt.Ltd, a leading pharmaceutical company located in Bangalore, India, specializes in manufacturing and exporting finished formulations across various therapeutic segments, including psychotropic and controlled substances. The company is dedicated to providing high-quality products and...

Company DescriptionGSS Pharma Pvt.Ltd is an emerging pharmaceutical company based in Bangalore, India. With a focus on manufacturing and exporting finished formulations, GSS Pharma caters to a diversified pharmaceutical market with over 400 formulations in therapeutic segments, including psychotropic and controlled substances. Committed to delivering quality...

The opportunityTo perform the case processing and related activities in alignment with patient Safety Operations.How you'll spend your day Processing serious & non-serious adverse events from various post-marketing sources Ensure accurate and consistent medical coding through MedDRA (Medical Dictionary for Regulatory Activities) for all events in Safety...

The opportunityTo perform the case processing and related activities in alignment with patient Safety Operations.How you’ll spend your day Processing serious & non-serious adverse events from various post-marketing sources Ensure accurate and consistent medical coding through MedDRA (Medical Dictionary for Regulatory Activities) for all events in Safety...

The opportunityThe Global PV Clinical Operations team member is primarily responsible to ensure case processing for safety information received from pre-authorization studies (clinical trials) is conducted in accordance with world-wide regulatory requirements, industry best practices and Teva internal processes and procedures The Global PV Clinical...

Roles and Responsibilities- o Review and verification of appropriate sections of adverse events, appropriate MedDRA coding, labelling, causality and provide a medical assessment comment as needed for ICSR.- o Reviews medical content and quality of the Case and ensures that all events from the source documents are accurately coded and verify consistency...

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that's bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation,...

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation,...

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation,...

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation,...

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that's bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation,...

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that's bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation,...

**Roles and Responsibilities** - o Review and verification of appropriate sections of adverse events, appropriate MedDRA coding, labelling, causality and provide a medical assessment comment as needed for ICSR. - o Reviews medical content and quality of the Case and ensures that all events from the source documents are accurately coded and verify consistency...

We are currently seeking a Junior MICC Associate to join our growing team. Working within the Medical Information Contact Centre (MICC) for the Pharmacovigilance function you will: - Follow both global and local regulations to protect personal and client related data as per company policy. - Be required to always exhibit a detail-oriented etiquette and...

**Primary Duties and Responsibilities** - Understand and interpret clinical trial study protocols to design and develop calendars. Understand and interpret clinical trial agreements and sponsor budgets to develop site budgets for the protocol. - Design and develop case report forms for clinical trial study protocols - Develop a familiarity with Advarra’s...

Department : Global Safety GBS (GS - GBS). Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can-do attitude with continuous improvement as one of your career objectives? Then we might...