pharmacovigilance associate

Pharmacovigilance Associate - VIE ContractLocation: Singapore, SingaporeTarget start date: 01/03/2027Program: iMove, the Sanofi VIE ProgramEligibility: Citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28. Applicants must submit applications in English.About the jobAs Pharmacovigilance Associate VIE within...

Sanofi Singapore is seeking a Pharmacovigilance Associate on a VIE contract to join the Patient Safety & Pharmacovigilance team. You will assist with intake, processing and reporting of local ICSRs in full compliance with local and global safety regulations.You will collaborate with the Country Safety Head to provide PV education and training, support signal...

Pharmacovigilance Associate - VIE Contract Location: Singapore, Singapore Target start date: 01/03/2027 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28. PLEASE NOTE that since this program is primarily an international development program, candidates cannot...

Sanofi Aventis Singapore Pte. Ltd is seeking a Pharmacovigilance Associate on a VIE contract in Singapore.You will assist with PV responsibilities ensuring regulatory compliance for Sanofi products in Singapore and support the Country Safety Head in intake, processing and reporting of ICSRs in line with local and global safety requirements. Join Sanofi's...

IQVIA is looking to appoint a Medical Advisor/Associate Medical Director to be part of our Medical Services team to deliver medical, clinical and scientific advisory expertise in clinical research studies. You will support compliance with protocol execution from a medical and scientific perspective. Also, you will provide medical expertise during project...

IQVIA is looking to appoint a Medical Advisor/Associate Medical Director to be part of our Medical Services team to deliver medical, clinical and scientific advisory expertise in clinical research studies. You will support compliance with protocol execution from a medical and scientific perspective. Also, you will provide medical expertise during project...

IQVIA is looking to appoint a Medical Advisor/Associate Medical Director to be part of our Medical Services team to deliver medical, clinical and scientific advisory expertise in clinical research studies. You will support compliance with protocol execution from a medical and scientific perspective. Also, you will provide medical expertise during project...

IQVIA is looking to appoint a Medical Advisor/Associate Medical Director to be part of our Medical Services team to deliver medical, clinical and scientific advisory expertise in clinical research studies. You will support compliance with protocol execution from a medical and scientific perspective. Also, you will provide medical expertise during project...

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing...

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver...

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver...

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing...

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver...

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing...

The Director, QRM, Global QMS, R&D & PV QA is accountable for establishing, governing, and continuous advancing a robust, science- and risk-based Quality Risk Management framework across R&D & Clinical Safety Pharmacovigilance, Medical Affairs and associated quality system. This role serves as the global QA authority for quality risk management, providing...

The Director, QRM, Global QMS, R&D & PV QA is accountable for establishing, governing, and continuous advancing a robust, science- and risk-based Quality Risk Management framework across R&D & Clinical Safety Pharmacovigilance, Medical Affairs and associated quality system. This role serves as the global QA authority for quality risk management, providing...

Job Description About this role: The Regional Head Regulatory Affairs, APAC provides strategic leadership for the Regulatory Affairs organization across APAC, leading LOC Regulatory Affairs Heads and International Regulatory Leads to ensure a unified regional voice and effective execution of global regulatory strategy. The role shapes and drives APAC...

Job ID: 20394 Location: Clarke Quay Working hours: 9am - 6pm Salary: up to $4,500 (Depending on experiences) Job Description 1) Regulatory Affairs . Manage the life cycle of the existing product portfolio in Singapore and Malaysia, while supporting regulatory compliance and continuity of product supply. . Prepare, compile, review and submit high-quality...

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IQVIA is looking to appoint a Medical Advisor/Associate Medical Director to be part of our Medical Services team to deliver medical, clinical and scientific advisory expertise in clinical research studies. You will support compliance with protocol execution from a medical and scientific perspective. Also, you will provide medical expertise during project...