Clinical Safety Scientist

Individual Case Medical Review (ICMR)The Scientist Level Clinical Safety Scientist (CSS) is responsible for support of safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational product development programs across early and late-stage development. Assists the protocol lead in safety reporting activities for...

Job Description:Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory agencies. We are on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and...

Job Description:Individual Case Medical Review (ICMR)The Scientist Level Clinical Safety Scientist (CSS) is responsible for support of safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational product development programs across early and late-stage development. Assists the protocol lead in safety reporting...

The Position High performing senior specialist who leads signal detection, safety evaluation and risk management planning and activities for key Organon's _highly complex_ medicinal products and/or medical devices during clinical development and/or for postmarketing PV setting from a scientific perspective by active participation and contribution to, amongst...

The Position Supports the Global Pharmacovigilance and Safety Science (GPSS) team in the safety surveillance (e.g., signaling) and risk management (routine as well as additional risk minimization measures, Risk Management Planning) of assigned, more complex established brands products and/or key new asset products (devices and/or medicinal products)....

Job DescriptionThe PositionSupports the Global Pharmacovigilance and Safety Science (GPSS) team in the safety surveillance (e.g., signaling) and risk management (routine – as well as additional risk minimization measures, Risk Management Planning) of assigned, more complex established brands products and/or key new asset products (devices and/or medicinal...

Job DescriptionThe PositionSupports the Global Pharmacovigilance and Safety Science (GPSS) team in the safety surveillance (e.g., signaling) and risk management (routine – as well as additional risk minimization measures, Risk Management Planning) of assigned, more complex established brands products and/or key new asset products (devices and/or medicinal...

The Position Leads signal detection, safety evaluation and risk management planning and activities for lowmedium complex_, _medicinal products and/or medical devices during clinical development and/or for established brands from a scientific perspective by active participation and contribution to, amongst others, the Organon Asset teams (when available) Risk...

Job DescriptionThe PositionLeads signal detection, safety evaluation and risk management planning and activities for low-medium complex, medicinal products and/or medical devices during clinical development and/or for established brands from a scientific perspective by active participation and contribution to, amongst others, the Organon Asset teams (when...

Job DescriptionThe PositionLeads signal detection, safety evaluation and risk management planning and activities for low-medium complex, medicinal products and/or medical devices during clinical development and/or for established brands from a scientific perspective by active participation and contribution to, amongst others, the Organon Asset teams (when...

Job DescriptionThe PositionLeads signal detection, safety evaluation and risk management planning and activities for low-medium complex, medicinal products and/or medical devices during clinical development and/or for established brands from a scientific perspective by active participation and contribution to, amongst others, the Organon Asset teams (when...

The Medical Writing Department of the GCTO organization prepares various regulated documentation. The Senior Medical Writer Safety Services role focuses on participant safety reporting, such as participant narratives, that support the clinical and regulatory writing portfolio.The Senior Medical Writer Safety Services is responsible for developing and...

Job Description:The Director provides dynamic leadership and strategic direction with regards to high quality and excellent compliance of individual case safety reports (ICSRs) and, the performance and results of the Medical Safety Review (MSR) Physicians in the US and globally. This role has responsibilities for ensuring operational and scientific...

As a Drug Safety Associate you will be joining the world' s largest & most comprehensive clinical research organization, powered by healthcare intelligence.What you will be doing:A Drug Safety Associate is a professional who is an integral part of drug development lifecycles to collect accurate safety information and to ensure patient safety.- Receives and...

Job TitleMEDICAL SAFETY EXPERT About AbbottAbbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self...

Job TitleMEDICAL SAFETY EXPERT About AbbottAbbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self...

Job Description:The Principal Medical Writer Safety Lead is responsible for development and management of medical writing deliverables, with a focus on safety reporting, such as participant narratives, that support the clinical regulatory writing portfolio.Capable of working independently to achieve goals.In this role the Principal Medical Writer Safety...

Job Description:The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the Clinical Research Associate manager the person ensures compliance of study conduct with International Conference on Harmonisation Good Clinical Practice and country regulations, our company policies and procedures,...

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we "follow the science" that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for...

Job DescriptionThe Senior Specialist within the PV-operations Clinical Safety Strategy Operations team collaborates with MRL colleagues to provide operational and regulatory pharmacovigilance (PV) input for company processes and standards and software system configuration that impact trial adverse event (AE) reporting and management. Maintains PV global...