Biotech Jobs in Palo Alto, California

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288 Palo Alto, CA Biotech jobs found on Monster.

Jobs 1 to 20 of 288
THE POSITION The Manager, Regulatory Strategy will be responsible for registration and regulatory support of US commercial and development projects. This position may be located in either Palo Alto, CA or Philadelphia, PA. RESPONSIBILITIES Participate as an active member of a multi-disciplinary team to establish development and regulatory strategies for commercial products, late stage, and ear...
The Director, Medical and Scientific Writing, is responsible for writing and managing the completion of a broad range of documents in support of company products and projects. As a writer, this individual will craft document messages and write, substantively rewrite, and edit documents companywide for sense, clarity, accuracy, and effectiveness. As a director, this individual will manage project d...
Company Overview Relypsa, Inc. is a late clinical-stage pharmaceutical company leading the discovery and development of novel non-absorbed polymeric drugs for important applications in cardiovascular and renal diseases. Relypsa's lead product candidate is patiromer, a non-absorbed potassium binder, which is being developed for the treatment of hyperkalemia. The company was formed in 2007 and is b...
STATISTICAL ANALYST II Genomic Health, Inc. seeks the following position in Redwood City, CA: Statistical Analyst II. Responsible for performing data review, statistical programming and statistical analysis of clinical and genomic data for assigned projects and studies. EOE. Submit resume at www.genomichealthjobs.com. Must refer to Job ID 2014-3829. No phone calls....
Our Pharmaceutical client in the East Bay Area is looking for a Manufacturing Purification Associate II to join their team! Duties: Primarily support the validation implementation. Operate in clean room. Support and ensure compliance of routine procedures following established company policies. Troubleshoot equipment and manufacturing procedures. Routine maintenance of manufacturing equipmen...
Senior Director, Clinical Drug Safety Science Description General Position Summary/Purpose: The Sr. Director of Clinical Drug Safety Science is responsible for the medical oversight of global pharmacovigilance activities of clinical trials and product development. Telecommute option is available after 3-6 months on site in Sunnyvale, CA Key Accountabilities/Core Job Responsibilities: Provide ...
Company Confidential Sunnyvale, CA, 94086
Purpose of the Job: Ensure that the company is adhering to its Quality Policy and Quality System. Provides Quality Assurance support to new product development projects from the Concept Phase through the Market Release Phase. Most important responsibility is ensuring that product used for human use has undergone the requisite quality control checks. Major Duties and Responsibilities: · Function...
Our Pharmaceutical client in the East Bay Area is looking for a Manufacturing Technician II/III to join their team! Duties: · Support equipment start-up and validation efforts of commercial fill/finish line. · Responsible for cGMP commercial fill/finish line. · Working knowledge of final formulation and fill/finish procedures, materials, and equipment. · Support validation of equipment and pr...
Our client in the South Bay is looking to have a Research Associate II join their growing team! Responsibilities: Perform chemical and physical assays on drug substance and drug products. Collect, calculate, and compute data, analyze and submit interpreted results to supervisor for disposition; report abnormalities immediately; investigate and analyze and resolve problems within prescribed scop...
Regulatory Affairs Project Manager System One has engaged with a global client in Santa Clara CA in seeking a Regulatory Affairs Project Manager. In this opportunity the regulatory affairs professional must possess a broad knowledge of all aspects of the regulatory space. The incumbent will develop new regulatory policies and SOPs and ensure the proper people are trained on them. Providing key re...
Assist in monitoring and collecting data from sponsor initiated clinical study. RESPONSIBILITIES: Travel to clinical research sites to collect clinical data for publication Check the data for compliance with study/site protocol, consistency and quality assurance Post-process, analyze the collected data using various software tools Document and report the analysis results Work with Investigat...
As part of the iCAD/Xoft Clinical Affairs team, the Clinical Affairs Project Manager will be responsible for the coordination of all activities associated with the conduct of multiple clinical trials (develops study protocols, CRFs; supervises study tasks and mentors other CRAs; assists in the generation and oversight of trial budgets and contracts; and communicates trial status to management). In...
Please note this is a 1 year contract position Skills: Regulatory Affairs experience, FDA Quality/ Medical Device The client is looking for a candidate with Medical Device experience. Description: Represents Regulatory Affairs on product lifecycle teams by actively contributing to the development and implementation of regulatory strategies. Independently prepares and negotiates regulatory subm...
Sr Regulatory Affairs Associate (Advertising & Promotional Review) System One has engaged with a Top Client in a search for a Sr Regualtory Affairs Associate to join their team in Santa Clara CA. In this critical role, you will ensure Regulatory Labeling and Promotional Review Compliance is within guidelines set forth by cGMP (GxP) and FDA standards. Knowledge of OPDP (Formerly DDMAC) is also re...
AT&T is seeking candidates for a highly unique opportunity in the field of Data Science. The opportunity is to participate as a member of a small team with a simple objective. Given one of the largest data sets in the world â¦.. Innovate! We are assembling teams to drive new and innovative ideas to our business units. The teams will consist of Subject Matter Experts, Data Scientist, Business Anal...
AT&T is seeking candidates for the unique opportunity to work with our massive, heterogeneous, data set. Our group has been tasked with creating a culture within a culture; a new team with a startup mentality focused on making big data and its thoughtful use a company imperative. You will not be yet another cog in a large internet company with a pre-existing big data machine. You will not be drivi...
Big Data at AT&T comes with big opportunities for innovation. With access to one of the largest and coolest data sets available, youll gain insight into the way consumers think, feel and act. And together, well turn that knowledge into innovative solutions that change the world, day in and day out. Located in downtown Palo Alto, youll find yourself immersed in a start-up culture with the support ...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Senior Biologist Palo Alto, CA Unspecified Apply Apply Senior Biologist Palo Alto, CA Unspecified Apply Job Details If you are a Senior Biologist with experience, please read on! We provide a broad range of environmental services to our clients, including environmental permitting, impact analys...
Job Description & Qualifications Summary Ford Motor Company is moving into a new phase of its 100+ year history, one in which openness is at the heart of its future. The automobile is being redefined as a networked computing platform upon which an ever-evolving set of applications is being designed, allowing us to create exciting new consumer experiences. We are a research lab within Ford that ...
This is an exciting position with a clinical laboratory offering next generation diagnostics for disease stratification and therapy selection. This company offers a comprehensive menu of specialized, advanced diagnostic testing in the areas of cardiology, oncology, reproductive disorders, endocrinology and infectious diseases. The company deploys cutting edge molecular diagnostic technologies and ...

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