Pharmacovigilance Associate I

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 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...

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...

Position:IT Associate IPrincipal Accountabilities Provide firstlevel IT technical support by resolving simple technical issues Support for any monitoring related queries and report complex incidents to Monitoring lead (IT Associate II) Logs tickets related to program failures and takes them to closure Coordinate resolution of issues with the help of...

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,...

Regulatory Professional I - LabellingCategory:Reg Affairs & Safety PharmacovigilanceLocation:Bangalore, Karnataka, IN- Department:RA Labelling Projects & Planning-The position As a Regulatory Professional I Labelling at Novo Nordisk, you will be responsible for the following:Packaging Material Coordination: Collaborate with stakeholders across Regulatory...

Regulatory Professional ICategory:Reg Affairs & Safety PharmacovigilanceLocation:Bangalore, Karnataka, INDepartment: Global Regulatory AffairsPosition**- Furthermore, in the role you will also handle:Compile, review and submit pre-meeting packages for authority meetings. Handle change requests. Submission of regulatory files, response to health authorities...

Position:IT Associate IWhat You'll Be Doing Provide firstlevel IT technical 24/7 support by resolving basic to moderately complex technical issues related to program scheduling across Arrow's business critical systems. Coordinate resolution of issues as needed with Development and Level 2 Support Teams Escalation to Level 2 Support team as and when needed...

Job Title: Regulatory Affairs Associate ICareer Level - CIntroduction to Role:Join our International Regulatory Affairs Management (RAM) team as a Regulatory Affairs Associate I. This role offers an exciting opportunity to contribute to the development and approval of life-changing medicines for patients in international markets. As a Regulatory Affairs...

Job Title: Regulatory Affairs Associate I Career Level - C Introduction to Role: Join our Biopharmaceuticals R&D team as a Regulatory Affairs Associate I, where you will play a critical role in impacting patients in need. As a specialist, you will assist other members of Regulatory Affairs Management (RAM) and the Regulatory Therapy Area (TA) in...

PrimaryResponsibilities: 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 Clinical Trial...

Description Title QA Validation Associate Main Purpose: The Quality Assurance Validation Associate I is responsible for the oversight and implementation of the Marken Quality Management System (QMS), Marken Standard Operating Procedures (SOPs), processes, and policies required to manage validation life cycles, calibration and maintenance of...

Department – Finance GBS Are you experienced in purchasing system administration and support? Do you have a strong business acumen and excellent communication skills? We are looking for a Senior Associate I to join our Procurement GBS team in Bangalore. If you are ready for a new challenge and want to be part of a global organization, read on and...

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration,...

Department: Global Finance GBS – Accounting Tax and Treasury Do you have sense of urgency, ability to manage and prioritise multiple work requirement to meet deadlines? Are you flexible and enthusiastic to go beyond the given instructions to create business value? If so, Novo Nordisk awaits your application as a Senior Associate I. Apply today and join...

Vantive: A New Company Built On Our LegacyBaxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care...

Regulatory Professional ICategory:Reg Affairs & Safety PharmacovigilanceLocation:Bangalore, Karnataka, IN- - Department:RA CMC Diabetes & ObesityAbout the department RA CMC & Device Bangalore is an integral part of RA CMC & Device and comprised of +60 experienced professionals associated with key regulatory processes covering Chemistry Manufacturing Control...