Drug Development Jobs in Irvine
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Search Results - Drug Development Jobs in Irvine
AbbVie-Irvine
to augment expertise in the therapeutic area.
Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. May be asked to contribute...
resume-library.com -
BioDuro-Sundia-Irvine
solutions and exceptional services to our clientele for challenging preclinical and clinical trial projects. With capabilities spanning Drug Discovery, Development, and Manufacturing, it is no surprise that BioDuro-Sundia is a leading partner of choice.
Why...
workable.com -
AbbVie-Irvine
will provide strategic input for toxicology safety assessment activities related to drug discovery, drug development, regulatory, and marketing commitments. This position will support projects in Eye Care, Aesthetics, and Neurotoxins.
Responsibilities...
resume-library.com -
Hamlyn Williams-Culver City, 41 mi from Irvine
experts.
The ideal candidate will have drug development project management experience with biologics programs. We are looking to make this hire between the senior manager and the senior director level.
This person will work with external manufacturing...
mindmatch.ai -
Allergan Aesthetics-Irvine
applicable regulatory requirements related to the clinical studies, clinician reported outcomes, patient reported outcomes and global drug development. Specifically in the area of aesthetic toxin development.
Contributes to design, analysis, interpretation...
resume-library.com -
PrimeGen US-Santa Ana, 6 mi from Irvine
of regulatory processes and drug development, with proven adaptability in a dynamic, fast-paced environment
Key Responsibilities
• Oversee the preparation, review, and submission of regulatory documents, including INDs, amendments, BLAs, supplements, annual...
mindmatch.ai -
Katalyst Healthcares & Life Sciences-Irvine
preferred.
Solid experience implementing the latest CDISC SDTM / ADaM standards.
Familiarity with drug development life cycle and experience with the manipulation, analysis, and reporting of clinical trials' data.
Submissions experience utilizing...
resume-library.com -
AcuraStem Inc.-Pasadena, 35 mi from Irvine
and RNA therapeutics
• Have extensive expertise in neuroscience, neural development, neurological disease modeling, stem cell biology, molecular biology, screening and drug development
• Successful track record of delivering therapeutics into clinical...
appcast.io -
AbbVie-Irvine
Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as a clinical representative for key regulatory discussions.
Ensures adherence...
resume-library.com -
Arrowhead Pharmaceuticals-Pasadena, 35 mi from Irvine
knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research and medical writing standards; demonstrated ability to interpret and apply these guidelines to document writing...
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