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BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases We target diseases that lack effective therapies..
To prepare regulatory documents for submission to regulatory authorities within subject area clinical safety The Regulatory Documentation Scientist takes accountability for delivering regulatory documents working effectively and closely with key..
This role within the in-vivo biology team in the Translational Immunology department is responsible for assessing new therapies to treat serious human diseases The successful candidate will identify develop and..
Cancel L Scientist I / Scientist II Cellular Pharmacology Lyell Immunopharma, Inc. South San Francisco , CA 94080 Posted Yesterday Apply This Job is not relevant Tell us why At..
The Team Lead will report to the Director of Program and Delivery Management Team and will be accountable leading the delivery team for a specific channel and digital service (Media,..
The Scientist I/II, Analytical Development will work in a biopharmaceutical analytical development group responsible for analytical method development, method qualification/validation and QC transfer of active pharmaceutical ingredients (API) and drug..
We are seeking a highly skilled and motivated in vivo pharmacologist to lead efforts in oncology, inflammation, and immuno-oncology. The ideal candidate will have expertise in small molecule PK/PD studies,..
We are seeking a talented and motivated Associate Scientist in the Small Molecule Analytical Chemistry (SMAC) Department at Genentech to develop automation strategies for high-throughput experiment and pre-formulation, and analysis...
Store 15331-SAN FRANCISCO CA District 00839-SAN MATEO CA Shift Various Apply Job Objectives Provides pharmacy consulting services to customers regarding the effective usage of medications, awareness with drug interactions and..
Lead the tactical support efforts of early development clinical trials from a clinical science perspective. Requires clinical industry experience plus a BA/BS and five years of pharma/biotech experience. Temporary with..
Job Description: The CMC Regulatory Affairs Project Manager will be responsible for tracking the status of key filings for clinical and commercial programs for all global markets. Other responsibilities include:..
Responsibilities: A postdoctoral position is available in the Department of Early Discovery Biochemistry to investigate molecular mechanisms underlying complex biology. Active areas of research include structure-function studies of protein complexes..
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses..
u003Cbu003EPosition Overview:u003C/bu003Eu003Cbru003Eu003Cp style=MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px\u003Eu003Cspan style=mso-fareast-font-family: timesnewroman mso-ansi-language: en-us mso-fareast-language: mso-bidi-language: ar-sau003Eu003Cfont face=\ arialu003EIncumbent in this role has dual campus responsibility and is accountable for the planning and operational..
Purpose The Medical Director at Genentech puts patients and science at the center of all actions. They drive medical tactics aimed at maximizing medical progress for patients. They collaborate to..
Job Description Locations: Philadelphia, New York/New Jersey, Boston, Chicago, San FranciscoJoin Accenture and help transform leading organizations and communities around the world. The sheer scale of our capabilities and client..
Myriad Genetics, Inc Myriad is an equal opportunity employer and as such, affirms in policy and practice to recruit, hire, train and promote, in all job classifications without regard to..
BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies..
DescriptionrnrnThe Senior Regulatory Operations Associate will be responsible for functional activities related to US and global regulatory submissions as well as clinical and compliance documentation.rnrn Responsibilities:rnrnrntSupport submission activities associated with..
US Tech Solutions is seeking a â€œ CMC Regulatory Affairs Project Manager for a 6 months position with a client in Foster City/California/USA/94404 Responsibilities The CMC Regulatory Affairs Project Manager..
Requirements Entry level No Education Salary to negotiate South San Francisco Description POSTDOCTORAL RESEARCH FELLOW - EARLY DISCOVERY BIOCHEMISTRY South San Francisco California, United States of America Job ID: 201903-108680..
Biotechnology opened the door to new types of medicines based on nature's own building blocks. No company has done more to advance this revolution than Amgen & the company's broad..
Requirements Entry level No Education Salary to negotiate San Francisco Description At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together..