Jobs 1 - 16 out of 16 for Drug Safety Scientist

Serves as operational lead responsible for receiving, assessing, obtaining follow-up, processing, and reporting adverse drug events regarding company pharmaceutical, nutrition, and biological products. Participates in global data exchange with the Fresenius Kabi entities and other Fresenius Kabi USA...

Evaluate medicine safety and benefit-risk profiles across clinical development and post-approval activities. Prepare safety assessments and benefit-risk documentation for regulatory submissions. Interpret clinical and safety data for cross-functional decision-making. Support signal evaluation, risk ...

The Senior Scientist, Process Safety, Drug Substance New Chemical Entity (NCE) is responsible for evaluating, characterizing, and mitigating thermal and reactive hazards associated with pharmaceutical compounds, intermediates, chemical processes, and active pharmaceutical ingredient (API) manufactur...

Serve as the NDS Therapeutic Area Leader for Immunology, overseeing nonclinical development programs and post-marketing support. Deliver nonclinical strategies, risk assessments, and regulatory submissions. Provide scientific oversight for Immunology candidates and collaborate with various teams. Ma...

Represent Nonclinical Drug Safety on discovery research teams, define and oversee NDS strategy for programs, provide risk assessments for targets, collaborate with NDS staff to execute studies, and lead early development teams.

The Discovery Program Leader is responsible for defining and overseeing the NDS strategy for programs in all modalities from Target Identification through to the approval of First-In-Human enabling GLP toxicity studies. Responsibilities include providing risk assessments for targets, de-risking stra...

The Discovery Program Leader is responsible for defining and overseeing the NDS strategy for programs in all modalities from Target Identification through to the approval of First-In-Human enabling GLP toxicity studies. Responsibilities include providing risk assessments for targets, de-risking stra...

The Discovery Program Leader is responsible for defining and overseeing the NDS strategy for programs in all modalities from Target Identification through to the approval of First-In-Human enabling GLP toxicity studies. Responsibilities include providing risk assessments for targets, de-risking stra...

The Discovery Program Leader is responsible for defining and overseeing the NDS strategy for programs in all modalities from Target Identification through to the approval of First-In-Human enabling GLP toxicity studies. Responsibilities include providing risk assessments for targets, de-risking stra...

The Nonclinical Drug Safety Therapeutic Area Leader is responsible for advancing the vision and goals of NDS, overseeing nonclinical development programs, delivering nonclinical strategies, providing scientific oversight, and collaborating with various teams. The role includes strategic planning, ri...

The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. NDS, Non-Clinical Drug Safety, helps advance high-quality drug candidates into development by defining the non–clinical safety and selectivity of lead compounds. NDS employees evaluate Lead...

The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. Interns will work on evaluating lead candidates and preclinical toxicity of drug development candidates, providing mechanistic understanding of drug-induced toxicity, and assessing implicat...

The Senior Scientist, Process Safety, Drug Substance New Chemical Entity (NCE) is responsible for evaluating, characterizing, and mitigating thermal and reactive hazards associated with pharmaceutical compounds, intermediates, chemical processes, and active pharmaceutical ingredient (API) manufactur...

The Director, Drug Safety & Pharmacovigilance Scientist provides strategic and scientific leadership for safety surveillance, signal detection, benefit-risk evaluation, and risk management activities across Dyne’s development programs. This role characterizes and communicates the safety profiles of ...

The successful candidate is responsible for safety surveillance and development of aggregate safety reports in compliance with global drug safety regulations. Responsibilities include leading proactive signal detection activities, managing Aggregate Safety Reports, authoring safety documents, and co...

Utilize medical knowledge and operational expertise to ensure patient safety by performing medical assessment of adverse events, assembling up-front safety information, collecting quality follow-up, and ensuring medical information is included in cases for investigational and marketed products. Faci...