Sr. Clinical Programmer Jobs in Cupertino, California
Currently, there are no Sr. Clinical Programmer jobs available in Cupertino, 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.
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 ...
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...
Cepheid Sunnyvale, CA, 94085
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...
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 ...
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...
Director of Clinical Affairs Job Description The Director of Clinical Affairs is responsible for all U.S. and international clinical trials conducted by CapsoVision and assures compliance to all relevant local, national, and international regulations, guidelines, and ethical standards. The Director works closely with senior management to assess business objectivesand develop a clinical strategy ...
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...
RESPONSIBILITIES: · Maintenance, repair and calibration of materials analysis/characterization instrumentation including FIB/SEM, XPS, AES, SIMS systems and other associated lab equipment · Hands-on operation of dual-beam FIB/SEM and EDS analysis REQUIRED SKILLS & QUALIFICATIONS: · Industrial experience in vacuum technology and electronics · Experience with Zeiss FIB or SEM, Physical Electron...
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...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Clinical Laboratory Scientist San Jose, CA Full-Time $65,000 - $90,000 Apply Apply Clinical Laboratory Scientist San Jose, CA Full-Time $65,000 - $90,000 Apply Job Details If you are a Clinical Laboratory looking to join a great organization, please read on! Our client is a leader in diagnostic...
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...
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 ...
EMC Corporation Santa Clara, CA, 95051
A primary role for systems integration is the technical implementation of complex, high profile solution initiatives. Solution scope generally involves various storage and data repositories, data movement layers, analytics databases, APIs and application enablement. Projects will often be developed with a rapid prototyping or proof-of concept approach. Ability and demonstrated experience wor...
Hortonworks Palo Alto, CA, 94306
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...
eBay Inc. San Jose, CA, 95111
The Hardware Engineering Group within ebay Inc.’s Global Foundation Services (GFS) is responsible for innovation, disruption, and architectural excellence across ebay Inc’s global infrastructure. The Sr. Storage Architect is responsible in three main areas; Definition of the overall software and hardware defined storage strategy, physical product design and ebay implementation, and alignment with ...
El Camino Hospital Mountain View, CA
Current BLS certification required Current CA RN license required Applies nursing process and theories, as well as principles of psycho-social and physical sciences, in assessing, planning, diagnosing, implementing, evaluating, and modifying patient care. Strives for quality outcomes and innovative practice in accordance with the California Nursing Practice Act and the Hospital/departmental poli...
Get new jobs by email for this search
We'll keep looking and send you new jobs that match this search.
Upload your resume and let employers find you!
It's that simple!
Biotech Career Tools
Sr. Clinical Progammer
$22,000.00 - $78,110.00
Typical Salary for Sr. Clinical Progammer in Cupertino
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
Source: Monster.com Careerbenchmarking Tool
Sr. Clinical Progammer
Maintains clinical data by developing and implementing data management plans (DMPs); coordinating and monitoring data flow and data entry; preparing documentation and reports; supervising team members.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Attention to Detail
Dealing with Complexity
Maintains clinical data by coordinating and monitoring information flow to data entry; controlling data entry; evaluating clinical data; identifying inconsistencies; coordinating resolution of data problems; developing and implementing edit-check and auditing procedures.
Verifies programming by performing trial runs; modifying program language.