Sr. Clinical Programmer Jobs in Foster City, California

Currently, there are no Sr. Clinical Programmer jobs available in Foster City, California which match this search. You may wish to explore similar job titles on the Biotech jobs in California page or view related jobs below.
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Responsibilities: Support cross-functional Study Team within Clinical Operations with minimal oversight from the Sr. CTM and/or CPL Responsible for Clinical Operations deliverables to achieve study objectives and milestones within timelines and budget Responsible for vendor selection and management including CRO, IVRS, central lab and imaging vendor Provide input to the study budget and is res...
Our Client in the South San Francisco area is looking for an EDC Programmer to join their team! Duties · Responsible for the technical aspects of study builds · Serve as the primary point of contract for assigned study · Build eCRFS, edit checks, custom functions and derivation · Responsible for testing: Unit and UAT · Ensure database design follows company standards: eCRF, edit checks, cust...
A pharmaceutical client in the San Carlos, CA area is looking for a contract Sr. Clinical Trial Assistant to join their team! This would begin as a 4-6 month contract and there may be the chance that they position could be extended after that time. This would be an office-based position and the ideal candidate will have the following: Bachelors degree (if on CRA track – degree must be in scientif...
Responsibilities Responsible for the implementation of clinical trial activities as defined by the Study Management Team. Works closely with investigative site personnel, CROs, and other study vendors under the direction of a Sr. CRA or CPM. Works with Medical Monitor and CPM or Study Lead to select investigative sites, train investigators and investigative site staff, preparation of materials f...
Kelly Services South San Francisco, CA
Description Clinical Trial Manager II SSF, CA, Contract 3 years The Research and Early Development (gRED) contract Clinical Trial Manager (cCTM) provides support and/or leadership to one or more global Study Teams within an early development program(s) (i.e. phase I and II trials). The cCTM is accountable for activities ensuring high quality deliverables are within budget and timelines. Primar...
The candidate, working closely with his/her Clinical Project Manager, will have overall responsibilities for managing the full scope of clinical trials (protocol development to final report, regulatory filing and/or publications) and coordinating cross functional efforts in order to achieve study objectives and corporate goals. Responsibilities: Assists with managing defined aspects of clinical ...
Job ID: 00434630 Sr. Research Associate â?? Oncology Biomarker Development Who we are At Roche, 85,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, weâ??ve become one of the worldâ??s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity. A member of the Roche Group, Genentech has been at the foref...
Who we are At Roche, 85,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, weâ??ve become one of the worldâ??s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity. A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 30 years, using human geneti...
Hoffmann-La Roche Inc. South San Francisco, CA, 94080
We are seeking a highly motivated and independent Senior Research Associate to join the Oncology Biomarker Development group within Development Sciences. Our group is responsible for developing and implementing diagnostic biomarker strategies and state of art molecular and genomic assays/technologies for supporting Oncology programs within clinical development at Genentech. The successful candidat...
As part of our commitment to bring effective therapies to patients with cancer, we are seeking a motivated computational biologist to join a team focused on the development of personalized medicine for patients with malignant disease. Employing data from state-of-the-art genomic analyses, the bioinformatics scientist will discover & validate molecular signatures that predict clinical response to O...
Hoffmann-La Roche Inc. South San Francisco, CA, 94080
We are seeking a highly motivated Senior Research Associate to join the ITGR/NTA Pharmacodynamic (PD) Biomarker group within Development Sciences. Our group is responsible for designing, developing and implementing PD assays for programs in clinical development at Genentech in the disease areas of Inflammation, Autoimmune diseases, Virology, Metabolism and Neuroscience. The successful candidate wi...
Stanford University Stanford, CA, 94305
Stanford University Department of Genetics has an excellent opportunity available for a motivated and experienced clinical biocurator on the ClinGen project funded by the National Institutes of Health. This individual will collect and integrate data from scientific literature published by clinical and human genome research groups. They will be an essential project member interacting with national ...
Job Description Job Title: Sr. /Staff Scientist, Bioinformatics Job Location: South San Francisco, CA Req-ID: 18011 Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of $17 billion and 50,000 employees in 50 countries. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences r...
The Document Specialist assists with the management and associated processes (from study set up to archiving) of Trial Master Files (TMF) for clinical trials conducted within Clinical Development. This position typically reports to a Sr. Director or Director or in Clinical Development. Core responsibilities applicable for studies following current SOP's for our client's Trial Master Files: • Sup...
Our client in the South San Francisco area is looking for a Clinical Technical Editor to join their Medical Writing Department! Technical Editor Duties: - Formatting clinical regulatory documents, including tables and graphics, in MS Word 2010 according to company Style Guide and Medical Writing Style Guide - Working on a variety of document types to company and industry standards under aggres...
Our client in South San Francisco is looking for a Director of Clinical Science join their team! Responsibilities: · Accountable for clinical/scientific evaluation of in-licensing opportunities. · Participates in other corporate and clinical development activities. · Participates in clinical/scientific evaluation of in-licensing opportunities · Key contributor to the development and execution...
Based in South San Francisco, California, Onyx Pharmaceuticals is an Amgen subsidiary, engaged in the development and commercialization of innovative therapies for improving the lives of people with cancer. At Onyx, our success begins with our employees. The progress we have made as a company reflects the talents of the individuals who have come together to develop possible new therapeutics for tr...
Responsibilities will include: Directs a multi-functional study team in the day-to-day execution of clinical trials Partners with Clinical Operations management and Project Management to define study milestones and deliverables and executes to ensure timelines, budget and quality are met. Actively participates in CRO, site and vendor selection in order to ensure that trial responsibilities are ...
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...
Kelly Services South San Francisco, CA
Biosample Operations Manager SSF, CA, Contract 12 months The Biosample Operations Manager (BOM) is accountable for the execution of the biomarker strategy that includes the planng and coordination all operational activities required for the collection and delivery of clinical trial samples (Biomarker, PK and PD) for assigned studies. The BOM is an integral part of the Study Management Team (SMT)...

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Biotech Career Tools

Sr. Clinical Progammer

Salaries

$22,000.00 - $78,110.00
Typical Salary for Sr. Clinical Progammer in Foster City
(2876 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
51.5%
Master's
23.8%
Doctorate
7.1%
Some College Coursework Completed
7%
Associates
5.5%
High School
2.4%
(2117 Respondents)
Source: Monster.com Careerbenchmarking Tool
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