Drug Development Jobs in Fremont
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Search Results - Drug Development Jobs in Fremont
Stevenson Search Partners-Fremont
for a drug development professional passionate about translating innovative science into meaningful clinical outcomes.
Summary: The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well...
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Precision Point-Fremont
and strategic problem solving skills
Preferred
• Experience with oncology, rare disease, immunology, CNS, or other targeted therapeutic areas
• Hands on experience with PBPK modeling platforms and model informed drug development approaches...
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Stealth Startup-Fremont
You'll Do
• Perform bioinformatics analysis and provide drug development expertise for assigned work.
• Provide expert scientific feedback to AI researchers from leading labs, helping shape how AI models interpret drug discovery workflows...
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Takeda Pharmaceutical-Cambridge, 2674 mi from Fremont
with strong practical experience with global HA requirements, beyond EU/US. who has an understanding of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support. Who has a proven ability to understand...
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Meet Life Sciences-Fremont
Associate Director, Medical Writing (Hybrid - SF Bay Area)
We are seeking an experienced Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory documents in support of complex drug development programs...
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Takeda Pharmaceutical-Cambridge, 2674 mi from Fremont
management within the global project team. The QCP role works in partnership with the pharmacometrics lead to drive a MIDD path within each project.
• Leads strategic, scientific, and operational aspects of multiple drug development projects with a high...
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Medasource-Fremont
development
• Basic understanding of chemistry and drug development and relevant experience in biotech or pharmaceutical companies
Education/Certification(s)/License(s):
• Education: B.S./M.S./Ph.D. in Computer Science, Data Science, or a related field...
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Takeda Pharmaceutical-Cambridge, 2674 mi from Fremont
of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support.
• Proven ability to understand and communicate regulatory strategy to drug development, registration, and post-market support teams.
• Analyze...
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Proclinical Staffing-Fremont
Demonstrated success developing and executing global regulatory strategies and leading submissions across multiple stages of drug development.
• Deep knowledge of US regulatory requirements (FDA), with experience in ex-US markets (e.g., EMA, Health Canada, MHRA...
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Takeda Pharmaceutical-Cambridge, 2674 mi from Fremont
relevant to global drug development and post-market support.
• Proven ability to understand and communicate regulatory strategy to drug development, registration, and post-market support teams.
• Analyze issues with attention to detail.
• Base regulatory...
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Compass Consulting-Fremont
requirements, international regulatory guidelines, and the end to end drug development process.
• Travel: Some travel maybe required....
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Takeda Pharmaceutical-Cambridge, 2674 mi from Fremont
Quality Assurance can be considered.
• Understanding of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support.
• Proven ability to understand and communicate regulatory strategy to drug development...
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Porton Pharma Solutions Ltd.-Fremont
activities, and projects.
Knowledge & Skills:
• Good Knowledge of CMC, cGMP, API, and the drug development process for small molecules.
• Proven track record in selling products or services, with exposure to a variety of sales techniques applicable...
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Amber Bio-Fremont
in building a new frontier in genetic medicine, please apply via LinkedIn.
Job Description: Associate Director or Director, Nonclinical Development
Position Overview:
We are seeking an experienced and highly motivated Director of Nonclinical Development...
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Kelly-Fremont
Required:
• Bachelor’s degree (10+ years), Master’s degree (8+ years), or an equivalent combination of education and experience in pharmaceutical, biotech, or CRO drug development, in disciplines such as toxicology, pharmacology, biology, or biochemistry...
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