Clinical Programmer Jobs in New Jersey
CLINICAL SAS PROGRAMMER (MID-LEVEL) REQUIREMENT #13-01048 RECRUITER: CHERYL AMBROSE JOB LOCATION: LAWRENCEVILLE, NJ NOVEMBER 27, 2013 Project Description: MS or MA in computing, statistics, or related discipline Minimum of 4 years programming experience in pharmaceutical industry or with CROs Demonstrate experience is required in Phase I, II, and III clinical development with working knowledge of...
The Senior Clinical Applications Programmer will provide technical leadership with responsibility for delivering technical services and management of data streams of vendor data within the scope of assigned projects. This position is located in our Princeton, NJ office with an option to work remote. Job Requirements: • Technical leadership with responsibility for delivering technical services (EDC...
The Principal Clinical Database Programmer (SDTM) will act as lead DB programmer and interact with related teams. Position based in our corporate Headquarters in Princeton, NJ. Consideration for remote workers. Responsibilities: - Ensure quality of personal work and the work of the team when acting as a Lead DB Programmer - Interact with project team members in related disciplines e.g. Clinical Da...
SAS Programmer Summary The primary responsibilities of the Senior SAS programmer includes development and validation of SAS analysis datasets; writing, validating, generating and running customized and standard programs and macros for analyses, tables, listings and graphics from epidemiological studies and clinical trial data. The Senior SAS programmer will report the Associate Director, Statistic...
Klein Management Systems Woodcliff Lake, 07677
Biostat Programmer Contract position Woodcliff Lake, NJ 07677 To support the Biostatistics team by carrying out and overseeing programming activities of statistical programmers and external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies. Contributes to the overall efficiency and best practice running of the Biostatistics group, d...
We are looking for talented clinical research professionals for Intern, Statistical Programmer - 临床统计编程实习生in Covance Beijing office. If you Studying for a Bachelor/Master in a computing, life science, mathematical or Statistical subject and speak fluent Chinese, we want to talk to you about the Intern, Statistical Programmer opportunity. Clinical Data, Analysis, and Reporting Organization (CDARO)...
Excellent opportunity for an experienced Biostat Programmer! Fabulous work environment! Long-term contract opportunity! Biostat programmer Oncology PCU Main purpose of the job: To support the Biostatistics team by carrying out and overseeing programming activities of statistical programmers and external vendors (as required), and to ensure timely and accurate programming and validation activities...
Principal Programmer with extensive pharmaceutical or CRO industry and either SAS or adAM experience is needed to work in Princeton, NJ or Nashville, TN. Responsibilities: - Act as the Lead Programmer overseeing technical planning for increasingly complex projects including global and multiple study projects, Integrated of Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) and electr...
Senior Statistical Programmer 高级临床统计编程员 (Taipei/Beijing/Shanghai) http://jobsearch.covance.com/43640-jobs.aspx We are looking for talented clinical research professionals for Senior Statistical Programmer 高级临床统计编程员 in Covance Taipei/Beijing/Shanghai office. If you have years’ statistical programming experience on clinical trial and speak fluent Chinese, we want to talk to you about the Senior Stat...
. Adecco Engineering and Technical, a division of the world leader in the recruitment of scientific and engineering professionals, has a full time opening for a SAS Programmer with Pharmaceutical and Clinical Trials experience for a contract position in central NJ RESPONSIBILITIES: · The Statistical Programmer will provide specialized knowledge and support to carry out statistical programming acti...
Excellent opportunity for an experienced SAS Programmer Analyst! Very stable, fast-growing international pharmaceutical company! Long-term contract opportunity! Sr SAS Programmer Analyst Perform SAS programming to provide data review complex listings/reports to support Data Management function for Oncology trials. Develop programs for patient profiles and ad hoc reports for data review to support...
Job Title: Biostat Programmer Job location:- Woodcliff Lake,NJ-07677 Duration: 12 Months JOB DESCRIPTION: Biostat programmer Oncology PCU Main purpose of the job: To support the Biostatistics team by carrying out and overseeing programming activities of statistical programmers and external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical s...
Top Pharmaceutical/Biotechnology company Contract SAS Programmer (mid to senior level) Several openings North NJ, 1 year renewable contract (W2 basis, $50.00 to $80.00 phr depending on experience). Description: -Provide SAS programming support and validation to help set specifications of analysis datasets, pooled datasets, statistical tables, summaries, figures and listing for all phases of clinic...
Position Summary : The Principal Statistical Programmer is responsible for all programming aspects (including analysis datasets, pooled datasets, tables, listings, and figures) of individual Phase I – IV clinical trials and project level activities for drug/Life Science projects. The Principal Statistical Programmer provides technical expertise to offer consulting, training and mentoring other pro...
Position Summary : The Senior Statistical Programmer is responsible for all programming aspects (including analysis datasets, pooled datasets, tables, listings, and figures) of individual Phase I- IV clinical trial. Leads clinical trial studies and contributes to training and mentoring initiatives. Key Activities : Statistical programming o Create or review data specifications. o Program or valida...
Sr. SAS Programmer – Outcome Research (Bio-Statistician with SAS programming skills) 13-month contract position Location: Bridgewater, NJ Prepare, verify, and manage research data sets from administrative health insurance claims, electronic medical record databases, randomized clinical trials, or other sources as per provided specifications. Perform ad-hoc queries, statistical analysis, modeling,...
Responsibilities: Provide statistical programming support and validation and help set specifications of analysis datasets, pooled datasets, statistical tables, summaries, figures and listing for Phase II-IV clinical trials. Employ standardized programs where applicable. Provide input into planning documents such as protocol, validation plan, and report analysis plan. Provide outputs for clinical s...
Note: Only W2 candidates Job Description: Excellent communication capabilities. Must work on-site. Technical skills evaluation will be given during interview process. 5 years programming and 3 years clinical trials experience, including table listing and figure production required. Complete Description: Computer programming position working with clinical trials data. Provides programming support f...
PhD Statistics w/minimum 4-5 years of trials based sponsor/CRO experience. MS degree requires 8+ years. Previous Clinical Pharmacology study experience required. Selected candidate will provide protocol related statistical support including analysis plan development, CRF review, interim analysis and final Statistical reports. Will serve as Consultant to clinical study team and provide support to L...
Overview: Design, develop, evaluate and modify computer programs to analyze and evaluate clinical data. Recognize inconsistencies and initiate resolution of data problems. Create programs using statistical analysis system language, such as SAS, to support the clinical area. Implements data management plans designed to meet project and protocol deadlines; provides expertise in the design and develo...
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$48,000.00 - $117,000.00
Typical Salary for Clinical Programmer in New Jersey
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
Source: Monster.com Careerbenchmarking Tool
Maintains clinical data by developing and implementing data management plans (DMPs); programming, coordinating, and monitoring data flow and data entry processes; preparing documentation and reports.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Attention to Detail
Dealing with Complexity
Develops data management plan by studying project requirements; contributing data management information in the design and development of clinical trials, protocols, and report forms.
Verifies programming by performing trial runs; determining sources of problems; modifying program language as needed.
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