Clinical Programmer Jobs

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1000+ Clinical Programmer jobs found on Monster.

Jobs 1 to 20 of 1838
TechData is looking for Biostatistician/SAS Programmer/Statistical Programmer (Some can be telecommuting), Medical Writer, Sr. Clinical Programmer, Data Entry, Clinical Research Scientist, Sales Analytics, Clinical Data Manager inNorthern NJ.Please see below requirements and send your resume to: *****. TechData is a leading provider for temporary and permanent positions in...
TechData is looking for Biostatistician (Contract/permanent, or remote), SAS Programmer/Statistical Programmer (Some can be telecommuting), Clinical Programmer, Pharmacovigilance, Outsourcing Manager, Medical Doctor, Clinical Data Manager, Informed Consent Form Specialist, Clinical Research Scientist, Safety Scientistfor our pharmaceutical clients in Northern and Central NJ. Please see below requi...
Our client has an immediate opening for a Lead Biostatistical Programmer who will be responsible for processing clinical data required for statistical analysis of Phase I - III clinical trials, and leading project teams. Job Responsibilities: Conduct statistical programming work of clinical data using SAS Version 9 or above Ensure that all programs, outputs and documentation are consistent with...
TechData Service is interested to talk to you about open contract positions with our top pharmaceutical clients. Currently, we have openings for Clinical Research Scientist(Summit,NJ), Contract Statistical Programmer (Summit, NJ), On Call Phlebotomist (Andover, MA), Product Safety Data Coordinator and Coding Associate , Executive Assistant,Project Manager (WCL, NJ), Medical Writer – Phase I (Austi...
SAS PROGRAMMER WITH WINDOWS / UNIX EXPERIENCE IN CLINICAL / PHARMACEUTICAL INDUSTRY REQUIREMENT #15-00308 RECRUITER: BRIDGET BURNS JOB LOCATION: HOPEWELL, NJ MARCH 19, 2015 Project Description: As a member of the Clinical Pharmacology and Pharmacometrics (CPP) group in the department of Discovery Medicine and Clinical Pharmacology, candidate will use the SAS programming language in a Windows/...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Responsibilities will include, but are not limited to, the following: 1. Provide programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells. 2. Write SAS programs to generate derived analysis datasets, perform analysis, and TFLs. 3. Perform ad hoc flexible and rapid programming arising from questions generated from planned analyses and results. ...
SAS Experience in Pharmaceutical or equivalent: ≥ 5 years. Oncology experience preferred. Have good knowledge of statistical terminology, clinical data structure , clinical tests, medical terminology, regulatory standards and protocol designs. Strong SAS programming / Macros development / SAS graphs skills. Demonstrated proficiency in using SAS to produce derived analysis datasets and produce ...
An outstanding Medical Device company with years of experience and a rich history is looking to expand their team with a Senior Clinical Database Programmer. Essential: - Must be an expert in SAS - Experience in Oracle Clinical - Great Communication Skills - Minimum 5 Years experience as a Clinical Database Programmer - Experience working for a Medical Device company in the past Desired: -...
Partner with Inventiv Health Clinical as a San Diego based Pharmaceutical client in support of Clinical Studies. The Senior Statistical Programmer will work closely with lead programmer, biostatistician, and clinical data managers in a project aimed to integrate related clinical study data. This position will also support ad hoc analysis for other projects when needed. Understand study design and...
Job Description: § Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. § Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting. § Perform quality assurance procedures on work performed by others. § Dev...
Are you a mid-level SQL Programmer seeking to find a permanent position with an organization that can offer continued growth in the field of Technology? Learn more about how you can be a part of growing Clinical Research Organization that offers complete solutions for clinical trials. About the Clinical Data Programmer role within ICON: The Clinical Data Programmer will be responsible for creati...
Title:Clinical Database Programmer Location:Murray Hill, NJ Duration: Full time Job Description The Senior Clinical Database Programmer will lead the development and maintenance of database builds in support of clinical studies. Responsibilities · Build study databases including development of database specifications/definitions, programming of CRF layouts, programming of validation and deri...
Being that the Pharmaceutical market has been pretty tough lately, it is exciting to mention that there are 3, remote, principal level openings at a Global Pharmaceutical company where I am currently working with the Global head of programming. This team is looking to move quickly with a 1 Stage interview process and is offering fairly competitive pay rates. Apply today or send this to a friend ...
Founded in 1978, Universal Health Services, Inc. (UHS)* is one of the nation’s largest and most respected healthcare management companies, operating through its subsidiaries—acute care hospitals, behavioral health facilities and ambulatory centers nationwide. With more than 68,000 people employed by UHS subsidiaries, UHS’s business strategy is to continue to grow by building or purchasing healthca...
Regulatory affairs associate Deerfield, IL Minimum Requirements: § Clinical SAS experience. § Will need previous industry experience, At least 5 years of CRO or Pharma. Job Description: § Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. § Ensure analysis data and programming code meet regulatory an...
Ultimate Staffing Irvine, CA
Company Description On-site at a Global Medical Device Company headquartered in Irvine, CA Job Description Global medical device company is looking for a Clinical programmer to join their team in Irvine, CA. This is a 6-8 month, W-2 contract position and is open to some remote work, though candidate must be available to be on-site in Irvine on a weekly basis. Job Description/Responsibilities: ...
Ultimate Staffing Irvine, CA
Global medical device company is looking for a Clinical programmer to join their team in Irvine, CA. This is a 6-8 month, W-2 contract position and is open to some remote work, though candidate must be available to be on-site in Irvine on a weekly basis. Job Description/Responsibilities: Create and validate eCRF layouts per clinical study requirements for EDC studies. Program and test edit chec...
Statistical Programmer 2 (Quintiles, Inc., May work at Overland Park, KS headquarters or telecommute from anywhere in the U.S.) Program, plan and coordinate the following for complex studies: (i) the programming, testing and documentation of statistical programs for use in creating statistical tables and listing summaries, (ii) the programming of analysis databases and transfers of data for inte...
Dyax is a biopharmaceutical company focused on the development and commercialization of products for unmet medical needs while creating value for patients, employees and shareholders. We are driven by one unifying factor which is to improve the lives of patients. We currently market a product for the treatment of acute attacks of hereditary angioedema (HAE), a rare genetic disease. We also have an...

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