Clinical Programmer Jobs
If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of that and more! We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam International has one of the largest global footprints...
Employment Opportunity K&L Consulting Services, Inc. (www.klserv.com) isa CRO that has been providing end-to-end data management, statistics, programming and medical writing services to the Pharmaceutical, Biotech and Medical Device industries since 1995. Our headquarters arelocated in Fort Washington, PA. Currently we have an opening for a Clinical EDC Programmer - InForm.If you would like to be...
Our client is seeking a SAS Programmer in Plymouth Meeting, PA for a long term engagement, as they are experiencing continued growth. Responsibilities: Clinical programming Perform project related programming (safety data sets, tables, listings) Validation of other programs Prepare project documentation Conduct programming activities according to SOP and department programming guidelines Requireme...
Our San Francisco Peninsula Client has a need for both full time and a contract SAS Programmer, the ideal candidate will provide statistical programming support and validation of analysis datasets, create statistical tables, graphs and listings for clinical trial data and assist in developing software to support project teams analysis requirements. CDISC experience (i.e. SDTM & ADaM) desireable....
PRA International Multiple
The Clinical Programmer (CP) is responsible for accessing and assembling clinical data from a variety of sources, converting the data to tabulation datasets and creating derived datasets following industry and client specifications, and generating tables, figures and listings to support analysis. Knowledge of industry‐accepted standards, including CDISC SDTM and ADaM, is necessary as is the abilit...
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...
Sr. Statistical Programmer/Analyst Description: Designs, develops, evaluates and modifies computer programs to analyze and evaluate clinical data. Generates Study specific and ad-hoc clinical data listings, summary tables and figures. Key Accountabilities/Core Job Responsibilities: • Performs data analysis using primarily the SAS programming language for the summary and interpretation of clinical...
Mid – Senior Level SAS PROGRAMMER (for Clinical Trials) Outstanding opportunity for a Mid - Senior level Statistician. This is a full time perm position with a major corporation in the Northern California Bay Area that also offers •Excellent opportunities for growth within the company •Excellent salary, benefits, etc. Wouldn’t you rather spend the coming winter in beautiful and warm California? Mu...
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...
As a Staff Clinical Programmer you will support the creation and maintenance of clinical database structures, conventions, reports, edit specifications, software user instructions and other deliverables required during the life of a clinical study, to ensure regulatory compliance and data quality within our Transcather Heart Valve business. Responsibilities: Support the design, development, testin...
Sr. Clinical Programmer - San Mateo, CA (Multiple Direct Hire Positions) Looking for a rewarding career change with a top San Francisco biopharmaceutical employer? Use your Clinical Programming expertise to support multiple Therapeutic areas and 2-3 filings annually. Job Description: Clinical Support: Acts as lead statistical programmer for a project providing consistency and quality assurance acr...
Tasks & Responsibilities: A programmer responsible for implementing and coordinating the flow of clinical data into study databases. Analyzes and evaluates clinical data for inconsistencies and initiates resolution to data problems. 1. Design database requirements, specifications, and case report forms; including automated edit checks and indications of critical variables. 2. Develop documentation...
My name is Dillon and I represent The Fountain Group. We are a national staffing firm and are currently seeking a SAS Programmer for a prominent client of ours. This position is with a global medical company specializing in eye care products located in Fort Worth, TX. Details for the position are as follows; Length: 1+ years Pay Rate: $52.00 Qualifications Four-year degree in scientific discipline...
Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC) discovers and develops new compounds that address unmet medical needs and advance human health. OPDC has numerous compounds in development to treat disorders in the neuroscience, oncologic, and cardio-renal therapeutic areas. OPDC is part of the Otsuka Group companies. For more information, visit www.otsuka-us.com. Contributes to t...
This is an immediate need in San Francisco; will need local candidates. This is NOT CLINICAL SAS. Financial Industry experience. Marketing Database Contractor: We are looking for an experienced SAS/SQL programmer to maintain existing processes and create new ones that manage the database infrastructure for the campaign environment. This environment helps to deliver new direct marketing opportuniti...
Our Boston area Client has a need for a full time Lead SAS Programmer / Sr. Statistical Programmer. The ideal candidate will provide statistical programming support and validation of analysis datasets, create statistical tables, graphs and listings for clinical trial data and assist in developing software to support project teams analysis requirements. CDISC experience (i.e. SDTM & ADaM) require...
Job Title:Clinical Statistical Programmer Job Location:Wayne PA, 19087 Duration:6 Months (High chances of Extension) Primary Responsibilities: · Minimum 8 years of SAS programming experience in the pharmaceutical, biotechnology, and/or contract research organization industries · The Clinical SAS Programmer creates SAS programs in support of sponsor’s clinical trials according to SOPs and guideline...
1. Utilizes SOPs and guidelines, trial protocols, annotated case report forms, Oracle*Clinical study definitions, trial and project data handling rules and standards, and Statistical Analyses Plans in preparation for the programming of the Data Quality Review Plan (DQRP) and the safety and efficacy tables, listings and graphs (TLG) required for the Clinical Trial Report (CTR) and the associated An...
Brief Description: Clinical ProgrammingRequirements: Foundation knowledge of SAS/Base and basic SAS procedures Working knowledge of Microsoft Office products Strong communication skills BS/BA or equivalent degree preferred Supervisory Responsibilities: None Specific Job Duties: Perform project-related programming (safety data sets, tables, listings) Validation of other programs Prepare project doc...
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Healthcare Career Tools
$48,000.00 - $117,000.00
Typical Salary for Clinical Programmer
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
Enhances organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.
Maintains clinical data by coordinating and monitoring information flow to data entry; controlling data entry; evaluating clinical data; identifying inconsistencies; coordinating resolution of data problems; auditing procedures.
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