Clinical Programmer Jobs in New Jersey
Job Title: SAS Clinical Programmer Position Description Candidates must have strong SAS programming experience. Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions. Assumes protocol level and some project management responsibility while supporting the Programming and Statistics...
CLINICAL SAS PROGRAMMER (MID-LEVEL) REQUIREMENT #14-00131 RECRUITER: CHERYL AMBROSE JOB LOCATION: LAWRENCEVILLE, NJ FEBRUARY 20, 2014 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...
Long Term Experience Required: · Requires proficiency with SAS programming, macros, SAS/GRAPH, and SAS/STAT; · Three years of programming and clinical research or related experience · Proficiency with Database Management and PL/SQL · Knowledge of clinical trials and relational database structure · Proficient in one or more programming languages. Knowledge and Skills : · Excellent written and verba...
A leading company in the clinical research industry is currently seeking a Statistical SAS Programmer to join their team. For the right candidate, this is a fantastic opportunity with great growth prospects. Details: 1) Write SAS programs that produce analysis datasets (ADaM) and analyses specified (ADaM) in the Statistical Analysis Plan 2) Validate SAS programs that produce analysis datasets and...
SENIOR STATISTICAL PROGRAMMER REQUIREMENT #14-00150 RECRUITER: BRIDGET BURNS JOB LOCATION: HOPEWELL, NJ FEBRUARY 27, 2014 Project Description: Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions. Assumes protocol level and some project management responsibility while supporting...
Excellent opportunity for an experienced SAS Programmer Analyst! Long-term contract with a fast-growing international pharmaceutical company! Fabulous work environment! The SAS Programmer Analyst's role is to support the Oncology Data Management group by carrying out the following functions: • Work independently to provide complex data review Listings, Reports, Patient profiles and Edit checks for...
Excellent opportunity for an experienced Biostat Programmer! Long-term contract opportunity with a fast-growing international pharmaceutical company! Fabulous work environment! 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...
Job Title: Statistical Programmer Duties: Provide statistical programming support and validation and help set specifications of anlysis 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...
5 DAYS ON SITE WORK ONLY EXPERIENCE OF WORKING ON ONCOLOGY PROJECTS IN MEDICAL AFFAIR GROUP IS PREFERRED 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 h...
PRINCIPAL SAS PROGRAMMER ANALYST Phase I Experience Required *These remote opportunities are open to any US home-office location. Theorem Clinical Research is seeking Principal SAS Programmers for full-time positions supporting our sponsor’s biometrics project needs. In this role, the Principal SAS Programmer will serve as a lead programmer for projects; serve as contact with clients for programmi...
The Database Programmer II is responsible for providing technical services (Electronic Data Capture) on assigned projects to achieve project integrity and the delivery of on time, quality data. Job Details: • Perform all activities related to study build and design including preparing eCRF specification or annotated data capture instruments and screen development. • Participate in sponsor screen d...
Type : Front-Line, Experienced 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, t...
We're currently hiring for a biostatistical programmer for a leading, global pharmaceutical company. This exciting opportunity will give you the opportunity to spend a year on site at one of the most exciting pharmaceutical research centers in the world! You must be comfortable with the following requirements: Review protocols, statistical analysis plans and case report forms, and provide SAS data...
PRINCIPAL SAS PROGRAMMER ANALYST *These remote opportunities are open to any US home-office location. Theorem Clinical Research is seeking Principal SAS Programmers for full-time positions supporting our sponsor’s biometrics project needs. In this role, the Principal SAS Programmer will serve as a lead programmer for projects; serve as contact with clients for programming aspects of clinical studi...
This reputable company with multiple locations across the United States seeks a Senior Statistical Programmer for their growing group! This opportunity offers the candidate flexibility to work entirely from home. This role includes, but is not limited to: Leading multiple studies, and a small group of programmers Phase I - III clinical trial experience CDISC studies Working crossfunctionally with...
Leading Pharmaceutical services company has an opening for a SAS Programmer II- WORK REMOTE. Job Description Type Of Job: Full Time + Excellent Benefits Job Responsibilities: Responsible for the production of SDTM datasets to the required specification. • Produce Data Definition Documents (DDDs) and a CRF to the dataset. • Read-in and reconcile electronic data with the CRF. • QC datasets, DDDs, a...
Job Description: To Support the Oncology Data Management group by carrying out the following functions: • Work independently to provide complex data review Listings, Reports, Patient profiles and Edit checks for Clinical and DM team. • Participate in review process of study documents such as the annotated CRFs/eCRFs. • Design and develop SAS macros, small applications, and other utilities to exped...
Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clin...
Duties Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrat...
Key Activities : Statistical programming Providing support for creating and maintaining programs to analyze and report clinical trials data. o Create or review data specifications. o Program or validate derived datasets, tables, listings and graphs Providing quality control for study documents, programs and outputs of statistical programs Effectively contribute to department study teams. study Qua...
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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
Documents programming and data managing procedures; maintains libraries of validated programs, macros and procedures.
Develops data management plan by studying project requirements; contributing data management information in the design and development of clinical trials, protocols, and report forms.
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