Company Description We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North
Department : Global Safety. 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
•Should have skills – Pharmaceutical Industry Validation Testing Experience – IQ\OQ\PQ. Worked with ALM or any other test management tool. •User should have knowledge about MES – Manufacturing Execution System application and its navigation (Preferably Pas-X).
Are you an experienced primary market research (PMR) professional with a passion for generating and disseminating insights? Do you have ability to build compelling stories when presenting results? Are you ready to take on a global
Job Description To review medical records of claimant and provide precise summaries covering all relevant medical facts required for claim adjudication process. Ability to identify key morbidity and mortality factors for medical impairments esp post casualty
Prioritize case processing activities for ICSRs in accordance with project guidelines, Regulatory due date and TAT SLAs and KPIs. • Processing and evaluation of Individual Case Safety Reports • Consistent data entry and processing from source
Department: RA Rare Endocrine Disorders Are you passionate about ensuring regulatory compliance for early phase products and/or managing product life cycle and amendments? Do you want to play a crucial role in keeping patients safe and
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
Department – Centralised Monitoring Unit (CMU)- Bangalore 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
Department: RA Rare Endocrine Disorders Are you passionate about ensuring regulatory compliance for early phase products and/or managing product life cycle and amendments? Do you want to play a crucial role in keeping patients safe and
Manager – DD&IT Development Department Name – Global Safety Solutions Location- Bangalore We are looking for an experienced people leader to join DD&IT Development in GBS team. You will become a part of a growing team
Job Purpose: − Work with Global Safety for literature evaluation in Safety Evaluation and Risk Management (SERM). − Perform Safety literature assessment activities for signal detection and aggregate reports purposes in accordance with their procedures and
Job Overview The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance
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
Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical
Department – IT QA Office 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
Company Description AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives
At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for to join our
Job Purpose and Key Responsibilities: Provide support for Central Safety Department (CSD) literature screening activities for both ICSR and signal detection purposes in accordance with their procedures and regulatory requirements. Support SERM product specialists
Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world