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Clinical Programmer Jobs in California

12 jobs

TechData is looking for Biostatistician/SAS Programmer/Statistical Programmer (Some can be telecommuting, Clinical Programmer in San Diego , L.A., CA.Please see below requirements and send your resume to: *****. TechData is a leading provider for temporary and permanent positions in the pharmaceutical industry. TechData offers the most competitive pay rate and benefits in ...
Job Summary The Senior Clinical Programmer (Senior CP) works in concert with study implementation teams to define and develop listings and datasets, and edit checks to assist in data review of clinical trials. Senior CPs develop and document standard specifications for data handled by Clinical Data Management (CDM), and model and transform operational data into CDISC standard data. Senior CPs may...
Medivation, Inc. (NASDAQ: MDVN – www.medivation.com) is a publicly traded biopharmaceutical company located in San Francisco. We are currently seeking a qualified, highly motivated, experienced individual for the position of Senior Clinical Programmer We are currently seeking a qualified, highly motivated, experienced individual for the position of Senior Clinical Programmer. This position is re...
Job Summary The Senior Clinical Programmer (Senior CP) works in concert with study implementation teams to define and develop listings and datasets, and edit checks to assist in data review of clinical trials. Senior CPs develop and document standard specifications for data handled by Clinical Data Management (CDM), and model and transform operational data into CDISC standard data. Senior CPs may...
Specific Responsibilities Works collaboratively with Clinical Programmers, Statistical Programmers, Biostatisticians, Clinical Research, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for moderately complex clinical data acquisition, quality checking and reporting. Ensures completeness, correctness and consistency of clinical data and data structure acro...
The Sr. Clinical Programmer (CP) develops and maintains clinical study databases as a member of Clinical Data Management (CDM). Working in collaboration with Data Managers and functional service providers, they are responsible for providing quality study databases and ensuring that technical database designs and edit checks are representative of protocol specifications. The Sr. Clinical Programmer...
The Sr. Clinical Programmer (CP) develops and maintains clinical study databases as a member of Clinical Data Management (CDM). Working in collaboration with Data Managers and functional service providers, they are responsible for providing quality study databases and ensuring that technical database designs and edit checks are representative of protocol specifications. The Sr. Clinical Programmer...
Job Description: OVERVIEW: Essential Duties and Job FunctionsWorks collaboratively with Clinical Programmers, Statistical Programmers, Biostatistics, Clinical Research, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for moderately complex clinical data acquisition, quality checking and reporting. Ensures completeness, accuracy and consistency of clinical ...
Job Level: Associate Director, D1 Reporting Functionality: US Medical Affairs / Evidence Generation Department: DATA Group – DATA SOLUTIONS Reports to: Director, DATA Group, Evidence Generation Direct Reports: Clinical Programmer (E4, E5), Administrative Associate, Senior Administrative Associate Location: South San Francisco The Head of Data Solutions is accountable for all Clinical Program...
Division Healthineers Job Type Regular Business Unit SI - Strategy & Innovation Job Time Full-Time Functional Area SL - Science/Laboratory Experience Level Mid Level Req ID 157017 Required Education Masters Degree Location CA - Berkeley Required Travel 10% Division Description Siemens is a global technology powerhouse that has stood for engineering excellence, innovation, quality, relia...
Specific ResponsibilitiesThis role will immediately assume study lead data management responsibilities for 3-5 concurrent clinical trials, utilizing primarily the Medidata RAVE electronic data capture and management system. The selected candidate will manage trials in various stages, from planning, to set-up, conduct, closeout, and archiving, in high volume, while maintaining a high level of data ...
Specific Responsibilities Assists in implementing routine activities involving CDM interaction with other study management team members. Reviews study protocols and assists site coordinators, investigators, and field clinical staff in collecting routine data to meet the protocol requirements in a timely manner. Identifies, tracks, and resolves routine queries and issues. The point of contact f...