- Merck (North Wales, PA)
- …into simple readable form + Solid project management skills + Familiarity with clinical data management concepts + Strategic thinking - ability to turn ... **Valid Driving License:** No **Hazardous Material(s):** N/A **Required Skills:** Business, Business, Clinical Data , Clinical Databases, Clinical Site… more
- Geisinger (Danville, PA)
- …statistical support to clinical investigators. + Experienced SAS or R programmer for both data manipulation and statistical analysis. + Detail-oriented with ... support throughout all stages of the research process-from proposal development to data analysis and interpretation. Core members offer expertise in: * Refining… more
- Cytel (St. Paul, MN)
- Experienced Medidata RAVE programmer to maintain Rave URL and be the point of contact for other teams using Medidata applications such as CTMS, eCOA, Safety Gateway. ... and CRO programmers + Act as a liaison for data collection between Sponsor DM and Statistical Programming +...other Medidata applications + At least 12 years progressive Clinical Research Experience + Medidata Rave Certified Study Builder… more
- Geisinger (Danville, PA)
- …statistical support to clinical investigators. + Experienced SAS or R programmer for both data manipulation and statistical analysis. + Detail-oriented with ... support throughout all stages of the research process-from proposal development to data analysis and interpretation. Core members offer expertise in: * Refining… more
- Edwards Lifesciences (Irvine, CA)
- …draft CRFs (Case Report Form), databases and perform edit checks + Partner with clinical data management team to ensure that the databases is defined consistency ... and execute programs in SAS and serve as lead programmer . + He/she will take primary role in review...in programming, documentation, validation and review of summary tables, data listings, and graphs for inclusion in clinical… more
- Tufts Medicine (Boston, MA)
- …documentation of data files for all study team members and works with computer programmer to maintain data file system for each project. 12. Works closely to ... Projects duties: Supports the development of new products and innovation. Includes Clinical roles focused on research projects. Positions in this family perform… more
- Dartmouth Health (Lebanon, NH)
- … data literacy. This is the most senior position in the Healthcare Data Programmer Analyst track. This position supports the Dartmouth Cancer Center. ... Qualifications * Master's degree with 8 years of experience in clinical quality data analytics and reporting or the equivalent in education and experience… more
- Sanofi Group (Morristown, NJ)
- …**Main Responsibilities:** + Provide high quality input into the design of the clinical study (including protocol development), the setup and conduct of the study to ... make sure data are adequately captured and collected to answer the...quality control plan. + Perform and/or coordinate with study programmer the production of statistical analyses. Review and examine… more
- Ascendis Pharma (Palo Alto, CA)
- …(SDTM, ADaM), strong communication and leadership skills, and a deep understanding of clinical trial data and analysis workflows. This position is based in ... at least 7 years of relevant experience. + Proven experience as a lead programmer for clinical trials and complex technical projects. + Excellent knowledge of… more
- Queen's Health System (Honolulu, HI)
- …providing high quality, responsive customer service. * Collaborates with clinical /physician leaders on quality improvement initiatives to assess financial outcomes. ... * Identifies financial performance improvement opportunities and collaborates with clinical /physician leadership toward exploration/implementation of initiatives. * Provides leadership… more
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