senior clinical data management programmer description jobs
1-10 of 19 jobs "senior, description"
Job duration: 11 Months Start date: ASAP Description: Essential requirements are: - Bachelors... in SAS-BI - A good understanding of CDMS Oracle Clinical and/or Medidata RAVE databases and/or a good... understanding of CDM processes - Good Clinical Practice. Full job specification to review... If you would... Salary: £1 per hour + dependent on experience Job type: Contract Job skills: Pharmaceutical, clinical
Requirements: Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician
Contract: Contract 11 Months
Manageer, Clinical Data Management, Data Analyst, Data Management, Data Manager, Management, Senior... Responsibilities and duties: • Complete clinical data management services from phase I studies... and English. Experience and skills: • At least three years experience in clinical data management within a CRO... org.uk. ( Keywords: Pharmaceutical, Pharma, Clinical Research, Data, Data Management, Data Manager, Data
Requirements: (SALARY: 40K-50K EUROS) (BASED IN: FRANCE) Our client provides Pharmaceutical and Biotech companies with new alternatives for lowering the cost of clinical development. Within the framework of their expansion they are now looking for a senior clinical
Job duration: 6 months+ Start date: ASAP Description: CONTRACT: Senior SAS Programmer Phase I-IV... and throughout Europe. Inclusive of SAS programming, Statistical, Clinical programming, Data Management functions... Skills & Capabilities: *At least x yearsexperience as a SAS programmer supporting clinical trials... to specifications, analysis datasets, pooled datasets, listings, tables and figures for phase I-IV clinical
Requirements: Pharmaceutical, clinical trials, SAS programming, statistical programming, statistics, statistician
Contract: Contract 6 months+
Reporting Trial, Non-Clinical Project Activities, Life Sciences, Senior Statistical Programmer, Program... The Senior Statistical Programmer’s major activities are as follows: 1) Lead programming activities... Research, Senior Statistical Programmer, SAS Programmer, Statistician, Senior Statistics, Statistical Lead... Programmer, Statistician, SAS Programmer, Clinical Trials, Phase I-IV, Marketing, Statistical Programmer
Requirements: and enthusiastic SAS Programmer I would be interested in hearing from you.
Programmer, SAS Programmer, Statistician, Senior Statistics, Reporting Management, Program Statistician... SENIOR STATISTICAL PROGRAMMER (SALARY: IS NEGOTIABLE) (BASED IN: SWITZERLAND) Our clients aim... protocol, CRF and data structures tables, listings and figures for phase I-IV clinical trials... CV to ----@----.Keywords: Pharma, Pharmaceutical, Clinical Research, Senior Statistical
Contract: Permanent
documents produced by other functions (e.g. CRF, Data Management Plan etc) *Review SAPs from the programming... Job duration: 12 months + Start date: Description: Job Summary: Working for this major client, you... will ensure; *all programming outputs pertaining to individual clinical studies and ISS/ISE meet required... Global Biostatistics *Function as a Project Lead Programmer with the following key activities:* Represent
Requirements: Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician
Contract: Permanent 12 months +
United Kingdom
Principal Statistical Programmer-316639 Description The Principal Statistical Programmer... works closely with other members of the Biostatistics department as well as Data Management and Project... is a member of the Biostatistics team and plays a strategic role in clinical trial analysis and reporting... activities of other staff members the Principal Statistical Programmer also leads departmental initiatives
Experience: Senior Specialist / Project Manager
Job duration: Start date: negotiable Description: Senior SAS / Statistical programmers - Germany... . Provides technical leadership within the data management team including line management as required... programmer, clinical programmer, statistical programmer, clinical trials, pharmaceutical, UNIX, Germany... programmer, clinical programmer, statistical programmer, clinical trials, pharmaceutical, UNIX, Germany
Requirements: SAS programmer, clinical programmer, statistical programmer, clinical trials, pharmaceutical, UNIX, Germany
Contract: Permanent
on study design and description of clinical endpoints. - For allocated studies, write the draft statistical... analysis plan - Collaborate with data management to ensure a quality database: by reviewing the proposed... the clinical study report together with a detailed description of the statistical methods and a statistical... edit checks, identifying any areas where additional data checks may need to be built into reporting
Experience: Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostat
Requirements: Skill 1: Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, Skill 2: Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, Skill 3: Pharmaceutical
Contract: contract
the statistical sections. Review the sections on study design and description of clinical endpoints... . - For allocated studies, write the draft statistical analysis plan - Collaborate with data management to ensure... . - Prepare the data analysis for the clinical study report: review protocol deviations/violations, confirm... the biometric text: including the clinical study report together with a detailed description of the statistical
Contract: Contract