R & D Jobs in California

RSS

1000+ California R & D jobs found on Monster.

Jobs 1 to 20 of 3276
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Infusion Pharmacist Gardena, CA; Carson, CA Full-Time $95,000 - $140,000 Apply Apply Infusion Pharmacist Gardena, CA; Carson, CA Full-Time $95,000 - $140,000 Apply Job Details Infusion Pharmacist RPH Mon-Fri Staff Pharmacist Specialty Pharmacy We are looking for an experienced infusion pharmaci...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Statistician/ Modeler (User Acquisition Analyst) San Francisco, CA Unspecified Apply Apply Statistician/ Modeler (User Acquisition Analyst) San Francisco, CA Unspecified Apply Job Details If you are a Statistican/Modeler with strong analytical skills, please read on! Top Reasons to Work with Us...
TypeRegular Full-Time Job Code*LI-JL2 Overview: Mallinckrodt Pharmaceuticals is pleased to bring Questcor and its entire business into our company. The former Questcor organization will be known as the Autoimmune and Rare Diseases business within Mallinckrodt’s Specialty Pharmaceuticals segment. We will continue their focus on the treatment of patients with serious, difficult-to-treat autoimmu...
TypeRegular Full-Time Job Code*LI-AW3 Overview: Mallinckrodt Pharmaceuticals is pleased to bring Questcor and its entire business into our company. The former Questcor organization will be known as the Autoimmune and Rare Diseases business within Mallinckrodt’s Specialty Pharmaceuticals segment. We will continue their focus on the treatment of patients with serious, difficult-to-treat autoimmu...
TypeRegular Full-Time Job Code*LI-AW3 Overview: Mallinckrodt Pharmaceuticals is pleased to bring Questcor and its entire business into our company. The former Questcor organization will be known as the Autoimmune and Rare Diseases business within Mallinckrodt’s Specialty Pharmaceuticals segment. We will continue their focus on the treatment of patients with serious, difficult-to-treat autoimmu...
Type Job Code*LI-JL2 Overview: Mallinckrodt Pharmaceuticals is pleased to bring Questcor and its entire business into our company. The former Questcor organization will be known as the Autoimmune and Rare Diseases business within Mallinckrodt’s Specialty Pharmaceuticals segment. We will continue their focus on the treatment of patients with serious, difficult-to-treat autoimmune and inflammato...
TypeRegular Full-Time Job Code*LI-AB1 Overview: Mallinckrodt Pharmaceuticals is pleased to bring Questcor and its entire business into our company. The former Questcor organization will be known as the Autoimmune and Rare Diseases business within Mallinckrodt’s Specialty Pharmaceuticals segment. We will continue their focus on the treatment of patients with serious, difficult-to-treat autoimmu...
Provide technical writing and administrative services in support of instrument and software operator manuals, product inserts, labels, specifications, and training materials: Write and edit documents to support Labeling Development in compliance with ISO, cGMP, and FDA guidelines, working within established formats and templates. Document types include: specifications, SOPs, package inserts, gu...
Job Duties/Responsibilities: •Demonstrated knowledge of safety concepts, per ICH and FDA guidelines per drug safety reporting requirements. •Performs a review of ancillary documentation accompanying ICSR reports and identifies pertinent clinical information for incorporation into the case narrative. •Performs Data Capture and Quality Review for all molecules and serves as a back up for addition...
Job Title: RA I, CV & Metabolic Diseases Position Description Will perform in vivo and ex vivo experiments to assess pharmacodynamics and efficacy of novel therapeutics in the relevant disease models. He/she will be responsible for execution of standard CV and renal rodent methodology (surgical and non-surgical). Position Responsibilities Under supervisor's direction, he/she will design and ex...
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...
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...
We are looking for Validation Engineer for the leading biotech company is South San Francisco. Below is the job description. Interested candidates, please submit your resume to ***** or call (510) 353 1700 Ext. 231 to discuss further about this position. Job Description: Job Title Systems Engineer - Verification and Validation You will work in collaboration with R&D, Marketing and P...
The Staff Biostatistician performs data analysis, statistical experimental, design, sampling techniques, and sample size determination in support of product development, clinical trials, regulatory submissions, and product quality. The qualified candidate exercises independent judgment in developing methods, techniques, and evaluation criteria for obtaining results and will develop specialized sta...
Ted Pella, Inc. is a worldwide leader in the microscopy supplies and instrumentation field. We are seeking an OEM Manager who is responsible for assisting the Vice President of Marketing & Sales in driving sales growth through the design, development, and implementation of specialized OEM distributer channels. This position reports to the Vice President of Marketing & Sales. Job Description · De...
Description: • Provides input to the operational strategy and feasibility of clinical research studies, in partnership with development operations. • Responsible for the formulation of clinical development plans, trial design, protocols, amendments and conduct data review, analysis and interpretation. • Responsible for clinical research studies (methodology studies, biomarker studies, proof of ...
Pharmaceutical firm in downtown San Francisco has immediate opening for experienced QA Assistant Pay range is $30 to $40 depending on experience. This is a 90 day contract position, 40 hours per week Requirements: • Associate or Bachelor's degree in chemistry, life science, medical, or related field • Work experience (> 1 year) in a cGMP, GLP, or GCP regulated area, or relevant course-work • ...
3 days/week daytime. Tuesday-Thursday. JOB SUMMARY: The primary job responsibilities are preparing media according to strict quality standards and providing exceptional customer service. Safely operate processing equipment including autoclaves and glass washers and report any issues. Work effectively and efficiently in a team-oriented environment to keep Media Prep operations running smoothly. Or...
BioPhase Solutions specializes in recruiting top talented professionals for California's Scientific community. We are recruiting for a Global Project Manager for our biotechnology diagnostic client located in Pleasanton. This is a long term contract role. Project Manager - Biotech Diagnostics Responsibilities: Leads in the creation of the Life Cycle Team (LCT) project plan, ensuring that the pl...
Pharmaceutical Data Project Manager Seeking a motivated, data-driven and analytical individual to manage the Clinical Operations data assets of this leading Bay Area biotechnology company. Use your project skills to provide standardized, high quality and accurate information for our Early Phase Clinical Trial Teams. - Use your cross-functional interactions with Data Quality Management, Program M...

Get new jobs by email for this search
We'll keep looking and send you new jobs that match this search.
email me

Upload your resume and let employers find you!
It's that simple!

Popular R & D Articles

5 Critical Elements of Any Résumé Article Rating
Including these five résumé elements will help you clarify your thinking, focus on key skills and accomplishments, and craft a résumé that will help you stand out from the crowd.
Steer Clear: Three Coworkers to Avoid Article Rating
Even if you try to get along with everybody, there are some coworkers you should just plain avoid. But what can you do when avoiding them not an option?...
For Employers: Post Jobs | Search Resumes | Advertise
About Monster | Work for Monster | Advertise with Us | AdChoices | Partner with Us | Investor Relations | Social Media
Terms of Use | Privacy Center | Accessibility Center | Help | Security | Contact Us | Sitemap | Mobile
©2014 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2014.4.45.50-210
eTrustLogo