Sr. Clinical Programmer Jobs in Palo Alto, California

Currently, there are no Sr. Clinical Programmer jobs available in Palo Alto, 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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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...
The Clinical Data Manager will be responsible for Data Management activities that support Jazz Pharmaceuticals’ commercial and development projects worldwide. He/she will participate as an active member of a multi-disciplinary team to plan and execute the Data Management tasks required for phase 1-4 studies. The Clinical Data Manager hasa broad, fundamental knowledge of the data management process...
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 ...
ATR International has been a leader in the staffing industry since 1988, placing professionals in the industry's most innovative companies. We currently have an exciting opportunity for a Sr. Scientist III with one of our important clients. Position Information: Job Title: Sr. Scientist III Location: Redwood City, CA Duration: 6 Months Compensation: DOE Contact Information: Kristy Huynh: kr...
Job Description: The Senior Clinical Research Associate will design, plan and implement the overall direction of clinical research projects. The primary responsibility is to assist the study team with all operational activities for new and/or on-going infectious disease and cancer diagnostic test product clinical evaluations. Responsibilities: •Independently responsible for all activities of th...
Our client in the East Bay is looking for a Sr. Manufacturing Associate to join their team! Sr. Manufacturing Associate Duties: - Train in fill-finish area of manufacturing and provide support as needed in all areas of manufacturing, including fermentation, purification. - Become a processing and equipment expert and serve as a hands-on resource in Production. - Perform routine procedures fol...
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 Summary: This position will interface with Global Clinical Affairs, Regulatory Affairs, Government Affairs, and Marketing to assure that development and clinical studies are appropriately represented in regulatory registration submissions and marketing collateral. This position reports directly to the EVP, Chief Regulatory Officer. Responsibilities: Assure that the appropriate R&D validatio...
Our client in East Bay is looking to have a QC Analyst join their team! Responsibilities: Regularly apply basic theory and principles from one's expertise in biochemistry, cell biology, and cGMP to develop, optimize, and validate physico-chemical and biological assay for lot release and stability testing. Participate in the technical transfer of assays to and from contract test laboratories und...
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...
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...
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...
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 ...
The Clinical Project Assistant will be a member of the Jazz Pharmaceuticals Clinical Operations team. The Clinical Project Assistant’s responsibilities include (but are not limited to) the following: General administrative support to the Clinical Project Teams Assist project teams with study specific tasks Ensure trial master files are current and maintained Co-ordination of Investigator paym...
The Director/Associate Director, Clinical Operations will lead a team of clinical operations professionals (Clinical Trial Managers, CRAs, Clinical Trial Coordinators) while being involved in the daily operations of Jazz Pharmaceuticals’ clinical programs. S/he will provide vision, leadership, and mentoring to their assigned team. The Director/Associate Director, Clinical Operations will lead a t...
The Clinical Trials Manager (CTM) will be a member of the Jazz Pharmaceuticals Development Operations team. The Clinical Trials Manager responsibilities include (but are not limited to) the following: Manage external vendors and contract research organizations Prepare study documents such as the Monitoring Manual, Study Operations Manual, Source Data Verification Plan and Laboratory Manual Coor...
CCS Associates has more than 25 years of broad-ranging experience providing expert consulting services to government and industry clients concentrating on acquisition and analysis of scientific information and on providing support at key steps of drug development. We are highly qualified in regulatory affairs, clinical and preclinical studies management, quality assurance, data management, data an...
Job Title: Clinical Trial Associate Position Description The in-house Clinical Trial Associate will serve to support the Clinical Operations team in all study related activities. Position Responsibilities Assist with logistical support for a clinical program and associated clinical trials. Delivery of complete TMF for assigned studies or program. Collection, review and tracking of regulatory...
The Hortonworks Release Engineering team is looking for talented and passionate engineers to create and deliver next-generation processes and tools for build, release, deploy, and configuration of our massively distributed computing platform, the Hadoop ecosystem. We’re passionate about open source, and ensure that all 100% of code in a HDP release is open sourced in the Apache Software Foundati...

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Biotech Career Tools

Sr. Clinical Progammer

Salaries

$22,000.00 - $78,110.00
Typical Salary for Sr. Clinical Progammer in Palo Alto
(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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