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Sr. SAS Programmer (2 x openings): Develop and validate complex SAS programs to analyze, manage and interpret large-scale clinical data. Produce and validate complex clinical trial reports, SDTM & ADaM datasets and TLGs to support FDA submission. Req: Master's degree /equivalent in Statistics, Bioinformatics, Computer Science or related field. SAS Clinical Trials Programmer Certificate. SAS Advanced Programmer Certificate. Send resume to TechData Service Company LLC, 700 American Ave., Suite 102, King of Prussia, PA 19406.
Biostatistical Programmer (2 x openings) in King of Prussia, PA: develop and validate complex SAS programs to analyze, manage & interpret large-scale clinical data. Produce and validate complex clinical trial reports, SDTM & ADaM datasets and TLGs to support FDA submission. Req.: Master's degree/equiv. in Statistics, Biostatistics or related, 1 year of experience in SAS programming and data analysis for clinical studies. Send resume to Techdata Service Company LLC, 700 American Ave, Suite 102, King Of Prussia, PA 19406.
Statistical & Scientific Programmer (2 x openings) in King of Prussia, PA: Perform statistical analysis and scientific programming to support pre-clinical and clinical research projects for drug discovery and development; develop scientific programming codes to conduct molecular simulation and rational drug discovery; design, develop, implement and validate complex SAS programs to process, analyze and report clinical data, generate datasets, TLGs etc. Req: Master degree or equiv. in Statistics, Biostatistics, Biochemistry, Chemistry or related; strong skills in SAS programming for new drug development. SAS Base Programmer Certificate. Send resume to Techdata Service Company LLC, 700 American Ave, Suite 102, King Of Prussia, PA 19406.
Title: Statistical Programmer Location, King of Prussia, PA Core Job Responsibilities: • Design, develop, implement and validate complex SAS programs to process, analyze, manipulate and report clinical trial data, including data extraction, program listing, generating datasets and tables. • Analysis, developing, testing/Validation, running, documentation and maintenance of SAS programs and macros to generate SAS datasets, spreadsheets, data listing, tables, and graphs and conducting statistical analysis of clinical trials data. • Provide data analysis and statistical programming for the clinical trial studies using Base SAS and advanced SAS Techniques. • Perform ad hoc flexible and rapid programming support to questions from Drug approval agencies. • Utilize CDISC guidelines to build datasets. • Generate outputs and reports to support other departments. • Perform all aspects of analysis, design, development, testing resolves programming problems and determines appropriate solutions. • Participate in the development and review of study-specific procedures; participate in project team meeting as required. Job Qualifications: • Bachelor’s degree in life sciences, statistics, pharmaceutical science, mathematics or related degree with mathematical or science backgrounds. • 5 plus years of proficiency in SAS programming • Demonstrated proficiency in using SAS to produce derived Analysis datasets(ADaM) and produce TFLs. • Lead experience in Pharma. • Good knowledge of medical terminology, clinical tests & drug development process. • Good interpersonal, communication, writing and organizational skills.
Biostatistician (2 x openings) in King of Prussia, PA: write and review SAP and clinical study protocol; provide biostatistical guidance on study design, statistical models, sample size recommendation, and data interpretation in clinical trials; Perform statistical analysis, write SAS codes to create and validate statistical summary reports and TLGs to support FDA submission. Req: Master degree or equiv. in Biostatistics, Statistics, Public Health or related. Strong skills in SAS modeling, data mining and analysis datasets. SAS Advanced Programmer Certificate. Send resume to TechData Service Company LLC, 700 American Ave., Suite 102, King Of Prussia, PA 19406.
Statistician (2 x openings) in King of Prussia, PA: write/review clinical research protocol, SAP, and study report for clinical trials; Develop & validate statistical models & SAS programs for analysis, management & reporting of large-scale clinical data, perform statistical and ad-hoc analyses to generate clinical trial reports and TLGs to support FDA submission. Req.: Master degree/equiv in Applied Statistics, Biostatistics or related, strong skills in statistical analyses (linear regression analysis, survival analysis, logistic regression analysis) and statistical modeling using SAS techniques. Send resume to TechData Service Company LLC, 700 American Ave., Suite 102, King of Prussia, PA 19406.
Sr. Clinical Data Analyst (2 x openings) in King of Prussia, PA: Provide complex statistical programming, data analysis and data mapping to support clinical trials and FDA submission for new drug development. Create and validate safety and efficacy LTFs and analysis datasets (SDTM, ADaM). Develop and modify data management and report forms in Phases I- IV of clinical trials. Req: Master degree/equiv in Statistics, Health Informatics or related, strong skills in clinical data analysis and reporting, SDTM & ADaM datasets. SAS Advanced Programmer Certificate. Send resume to TechData Service Company LLC, 700 American Ave., Ste 102, King of Prussia, PA 19406.
SAS Programmer (2 x openings) in King of Prussia, PA: develop and validate SAS programs to analyze, manage and interpret large-scale clinical data. Produce and validate complex clinical trial reports, SDTM & ADaM datasets and TLGs to support FDA submission. Req.: Master degree /equiv. in Statistics, Computer Science or related, strong skills in SAS programming for clinical studies. SAS Base Programmer Certificate. Send resume to TechData Service Company LLC, 700 American Ave., Suite 102, King of Prussia, PA 19406.
TechData is looking for Sr. Statistical Programmer to join our SAS Programming team to independently work on the assigned clinical research projects for our clients. As Sr. Statistical Programmer, the candidate will collaborate with cross functional team members and provide statistical programming support for clinical trials. Specific duties as follows: • Provide SAS programming support to Biostatisticians, Data Management team and FDA submissions. Participate in the review of Statistical Analysis Plans (SAP) and clinical study protocol, CRF, and statistical methodology, statistical programming procedure, analysis file specification, etc to ensure SAS codes are compliance with the requirements of SAP and study protocols. • Develop and validate complex SAS programs to create analysis datasets, tables, graphs and listings (TLGs), generate CDISC SDTM and ADaM datasets, including proper validation, testing and documentation for phase II-IV studies, and also provide programming specifications for CDISC SDTM and ADaM datasets. • Create and modify standard SAS macros for validation, analysis and generation of clinical reports; provide high quality statistical analyses support for the clinical trial studies using solid statistical theory and SAS/STAT/MACRO/GRAPH/SQL techniques. • Gather, analyze and interpret safety and efficacy data that are collected during clinical trials, and review data collection and management methodology and assure acceptability and scientific integrity of data collection and analysis through appropriate application of statistical principles and methodology. • Use statistical techniques to analyze the clinical data and generate Ad-hoc safety summary reports for review by research scientists and medical directors. Be responsible for checking whether the data are out of range of any safety guidelines provided by FDA or other agencies, and communicate with project manager and notify clients in a timely manner on any abnormal testing results. • Participate in preparing clinical study results for FDA submissions using SAS, writing intense QC documentation for every stage of reporting from extraction to the final reporting of the tables, and work closely with project manager and other team members, assist in client’s inquiries on clinical trial related statistical analysis with developing SAS techniques/tools. Qualifications/requirements: We require the candidate to possess at least bachelor degree or equivalent or higher in Statistics, Mathematics or quantitative related fields such as Financial Engineering. The candidate must have extensive knowledge of statistical modeling, probability theory and its applications, and strong skills and extensive work experience in statistical programming, manipulating and analyzing large scale of data, creating and validating datasets, producing and validating reports for clinical trials. Please send resume to TechData, 700 American Ave, Suite 102, King of Prussia, PA 19406, Attn: HR
Statistical Programmer (2 x openings) in King of Prussia, PA: Perform statistical programming to produce and validate analysis datasets (SDTM, ADaM) & TLFs for ISS and ISE in new drug development. Develop & validate complex statistical models, SAS programs/macros for analysis, management & reporting of large-scale clinical data. Req.: Master degree/equiv. in Statistics, Mathematics or related, strong skills in SAS programming and statistical analysis for phase I-III study. SAS Advanced Programmer Certificate. Send resume to TechData Service Company LLC, 700 American Ave., Suite 102, King of Prussia, PA 19406.
Biostatistician (2 x openings) in King of Prussia, PA: Develop and review SAP and clinical trial protocol; Provide statistical support for study design, data analysis, verification, and data interpretation in clinical trials; Create and verify clinical trial reports and TLGs to support FDA submission. Req: Master degree or equiv. in Biostatistics, Public Health or related. Strong skills in report generation, SAS modeling and data manipulation. Familiar with CDISC standards and analysis datasets. Send resume to TechData Service Company LLC, 700 American Ave., Suite 102, King Of Prussia, PA 19406.
SAS Programmer (2 x openings) in King of Prussia, PA: develop and validate complex SAS programs to analyze, manage and interpret large-scale clinical data. Produce and validate complex clinical trial reports, SDTM & ADaM datasets and TLGs to support FDA submission. Req.: Master degree /equiv in Statistics, Computer Science, Computer Engineering or related, strong skills in SAS programming for clinical studies. SAS Clinical Trials Programmer Certificate. Send resume to TechData Service Company LLC, 700 American Ave., Suite 102, King of Prussia, PA 19406.
Job Title: Programmer Analyst Job Summary: Programmer Analyst will work as a part of a multi-dimensional Analytical project team focused on delivering quality and timely deliverable for a variety of pharmaceutical and biotechnology clients. Programmer Analyst will need to play a key role in converting clinical trial data into knowledge and support development of medicines. The Programmer Analyst will build the appropriate programs in order to create datasets from the clinical database and other data sources as outlined in the clinical study's protocol, Clinical Data Management Plan, and/or Analysis Plan. The Programmer Analyst will develop SAS macros, templates and utilities for data cleaning, reporting and analysis. Programmer analyst will also support regulatory submissions. The Programmer Analyst will function without daily oversight in the performance of the specified duties. Job Duties and Responsibilities: • Review CRFs to ensure consistency with protocol and adequacy to collect the data to meet the objectives defined in the statistical section of the protocol. • Review CRF annotations and database data specifications • Creates derived-analysis datasets utilizing the ADaM standard of CDISC. Executes analyses specified in the protocol or the Analysis Plan under the guidance of the project statistician. • Works closely with the Biostatistics and Data Management members on various clinical projects. • Interface with Data Management and clinical to identify and program edit checks per the Data Validation Plan/Data Management Plan and study management reports using SAS. • Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming; • Write programs to generate SDTM domains, listings, and figures (TLFs) and analysis datasets (ADaM). • Perform validation of the programmed SDTM and ADaM as well as TLFs. • Create SDTM annotated CRFs as well as define.xml and reviewer’s guides to support electronic submission (eSUB) requirements. • Perform analyses defined in the statistical analysis plan as well as ad hoc analyses as requested • Preparing and validating submission packages, i.e. define.xml, Reviewers Guide • Applying your strong understanding/experience with Efficacy analysis; • Preparing submission packages • Performs all programming required for clinical trial analysis and reporting, and various other programming tasks • Demonstrates strong programming skills, participates in protocol team and some project team interactions. • Builds successful relationships and seamless interfaces at the protocol/project team level. • Provides timely and effective communication to the programming and statistics leads. • Participate in Vendor meetings (when appropriate) Job Requirements: • Minimum of bachelor degree in Computer Science, Computer Information System, Information Technology or related field etc. • Ability to provide quality deliverable, in adherence with challenging timelines. • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
TechData is looking for a full-time Statistical Programmer to work on the assigned off-site and in-house projects to support clients clinical study and new drug development. The candidate will collaborate with team member and provide high quality statistical analyses and programming support for the clinical trial studies and outcome research; manage, process, analyze and interpret safety data that are collected during clinical trials. Work closely with biostatistician, participate in the development and review of Statistical Analysis Plans (SAP) and statistical contributions, including statistical section of study protocol, CRF, and statistical methodology, statistical programming procedures, analysis file specifications, and tables, figures, and listings (TFLs) shells. Review data collection and management methodology and assure acceptability and scientific integrity of data collection and analysis through appropriate application of statistical principles and methodology. The candidate will use statistical techniques to analyze the clinical data and generate Ad-hoc safety summary reports for review by research scientists and medical directors. Also be responsible for checking whether the data are out of range of any safety guidelines provided by FDA or other agencies. Communicate with project manager and other team members and notify clients about any abnormal testing results. Develop and validate complex SAS programs to create tables, graphs and listings, CDISC SDTM and ADaM datasets, including proper validation, testing and documentation, produce and validate SDTM and ADaM datasets, listing and figures for multiple phase I-V studies. Create SAS programming specifications for SDTM and ADaM datasets, by following CDISC standards as well as clinical study specific requirements. In addition, the candidate will participate in preparing clinical study results for FDA submissions using SAS, writing intense QC documentation for every stage of reporting from extraction to the final reporting of the tables. Assist clients in their inquiries on clinical trial related statistical analysis with developed SAS tools and techniques. Req: at least bachelor or higher or equivalent in Statistics, Biostatistics, Mathematics, or Science related field. Please send resume to TechData, 700 American Ave, Suite 102, King of Prussia, PA 19406. Attn: HR
Statistical Programmer (2 x openings) in King of Prussia, PA: develop and validate statistical models and SAS programs to analyze, manage and interpret large-scale clinical data. Produce and validate complex clinical trial reports and TLGs to support FDA submission. Req.: Master degree/equiv in Statistics, Biostatistics, Mathematics or related, strong skills in SAS programming and data analysis for clinical studies. SAS Advanced Programmer Certificate. Send resume to TechData Service Company LLC, 700 American Ave., Suite 102, King of Prussia, PA 19406.
Statistical Programmer (2 x openings) in King of Prussia, PA: Provide statistical programming, data analysis and data mapping to support clinical trials and FDA submission related to new drug development. Create complex SAS programs/macros to generate and validate safety and efficacy LTFs and analysis datasets (SDTM, ADaM). Req: Master degree/equiv. in Statistics, Math, Information Technology or related, strong skills in SAS programming, data analysis, SDTM & ADaM datasets for clinical studies; SAS Advanced Programmer Certificate. Send resume to TechData Service Company LLC, 700 American Ave, Suite 102, King of Prussia, PA 19406.
Sr. Statistical Programmer (2 x openings) in King of Prussia, PA: Develop and validate complex SAS programs for creating TLGs & generating CDISC SDTM/ADaM datasets. Manage, analyze, interpret and report Phase I-III clinical trials data for FDA submission. Perform quality control checks of SAS codes and outputs produced by other programmers. Review SAP and validate clinical trial reports. Req.: Master degree/equiv. in Statistics, Biostatistics or related, with 1 yr of experience in SAS programming & data analysis for clinical study. Advanced SAS Programmer Certificate. Send resume to: TechData Service Company LLC, 700 American Ave, Suite 102, King of Prussia, PA 19406
TechData is looking for professional Biostatisticians to join our Biostatistics & Clinical Research team to independently work on the assigned in-house and off-site projects for our client clinical research projects. As Biostatistician, the candidate will collaborate with Biostatistics, Data Management, and Clinical staff to define and clarify clinical research project requirements, design and review statistical analysis plan (SAP) under guidance for all phases of clinical studies. Write and review clinical study protocols, statistical summary reports and Case Report Forms (CRFs) for proposed studies using statistical methodology. Review and assess clinical protocol deviations to the extent that they may affect statistical analyses. The candidate will analyze and interpret large-scale clinical data and produce statistical reports that may be incorporated into internal clinical reports or regulatory submissions. Use various statistical models to perform statistical analysis for planned and ad-hoc analyses and also write complex SAS programs to validate statistical results. The candidate will plan, produce and validate statistical and programming deliverables, and also validate the statistical deliverables produced by external vendors, and provide statistical guidance for the data management and statistical programming team. The candidate will coordinate and assist clinical research team with data and table reviews and other activities. He will apply statistical methodology to clinical trial design and analysis, and then draw conclusions or make predictions based on data summaries or statistical analyses. Work closely with project manager and other team members, assist our clients in their inquiries on clinical trial related statistical analysis and study protocols issues with developed SAS tools and techniques. Participate in the preparation and documentation of results to support clinical trials reports and publications. We require the candidate must possess at least a bachelor degree or higher in Biostatistics, Statistics or related discipline. Master's degree is highly preferred. The candidate must have extensive knowledge of biostatistics/statistics and strong skills in statistical data analysis, producing and validating reports for clinical trial projects. Please send resume to TechData, 700 American Ave, Suite 102, King of Prussia, PA 19406, Attn: HR
TechData Service Company, LLC in King of Prussia is looking for Senior SAS Programmer (Full-time): Design and develop complex SAS programs and Macros to create TLGs, ISS and ISE; generate and validate clinical trials data (SDTM&ADaM) and support FDA submission. The detailed job responsibilities include: Write complex SAS programs to validate and generate CDISC SDTM datasets and ADaM analysis datasets for multiple phase I-III studies based on SAP. Develop and validate complex SAS programs, SAS macros to create tables, graphs and Listings. Utilize programming skills within protocol team and perform all programming required for clinical trial analysis and reporting. Develop SAS coding and table templates for preparing, processing and analyzing clinical data. Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the data analysis plan, and conducting the actual analysis once a reporting database is created. Assist with the development of data analysis plans through collaboration with medical/statistical personnel. Provide SAS programming and validation support for clinical study reports, oversee programming activities by external vendors when necessary and coordinate programming activities to achieve timely progress. Work with external vendors in order to develop or monitor the content and structure of SAS data sets. Develop and implement solutions to improve programming efficiency and quality. Job Requirement: Master degree in Statistics, CS, EE, Engineering Management, or related fields plus 1year of experience in job offered. Additionally, 1 year of experience with each of the following skills is required: 1. Experience with: relational database structure; pharmaceutical clinical development including adhering to safety deliverables and performing efficacy analysis; project management; and creation of current CDISC data structures using SAS, SQL. 2. Knowledge of pharmaceutical clinical development and ability to provide programming support needs for FDA submissions for phase I-III study. 3. SAS Advanced Programmer Certificate. Job location: King of Prussia, PA. Please mail resume to TechData Service Company, LLC, 700 American Ave Ste 102, King of Prussia, PA 19406-4031
Biostatisticians (King of Prussia, PA) – Develop Statistical Analysis plan (SAP) under guidance for all phases of clinical studies; Design and review clinical study protocols and Case Report Forms (CRFs) using proposed statistical methodology, including survival analysis, categorical / longitudinal data analysis, sample size estimation; Write SAS programs to validate ADaMs and output tables, listings, and figures (TLFs); Write and review clinical study report (CSR); Design TLFs shell based on protocol, SAP, and clinical data collected from CRFs; Analyze and interpret output summary statistical tables, data listings, and figures for clinical trial data in ad-hoc reports using Advance Excel Functions; Validate SAS programs and analysis datasets using SAS9; Maintain documentation for SAS programs; Perform SAS9 programming for Clinical trial data in CDISC standard. Must have a Master Degree in Statistics or Biostatistics plus 2 years experience in job offered. Require skills and knowledge in SAP, CRFs, Clinical Study Report (CSR), SAS9 programming for Clinical trial data in CDISC standard, ADaM, Advanced excel functions, Survival Analysis, Longitudinal Data Analysis. Require 100% travel to unanticipated client locations in USA. Allow telecommuting. Job location: King of Prussia, PA. This position is eligible for Employee Referral Program. Send resume with job code SIH001 to HR, TechData Service Company, LLC, 700 American Avenue, Suite 102, King of Prussia, PA 19406.
TechData is looking for Statistical Programmers: Primary Duties and Responsibilities: • Program CDISC compliant SDTM and ADaM Datasets using SAS. • Program Statistical Analysis i.e., tables, listings, figures, and inferential statistical outputs using SAS. • Review Protocol and Statistical Analysis Plan (SAP) and write SDTM and ADaM Specifications. • Produce statistical reports using techniques such as SAS macro language, advanced data manipulation techniques, and statistical procedures (e.g., PROC GLM, PROC FREQ, PROC REPORT). • Perform quality control and review SAS programs generated by other statistical programmers and statisticians. • Review and provide feedback regarding electronic Case Report Forms (e-CRF) and Data Management Plans. • Create Define XML, Define PDFs, and Reviewers Guides. • Lead and work independently with minimum guidance and supervision. • Familiarity with coding dictionaries (WHO, COSTART, ICD-9, MedDRA) and with FDA regulations that affect the reporting of clinical trial data. Requirements: • BS equivalent in Computer Science, Statistics, Biostatistics, or related field. Master’s preferred. • 3+ years of experience in Computer Science, Statistics, Biostatistics, or related field preferred. • Excellent technical skills in Statistical Programming, with advanced knowledge in SAS, and other statistical computing software. • Excellent understanding of SOPs and industry regulations. • Strong organizational and communication skills. • Ability to multitask and prioritize work.
Biostatistician (2 x openings) in King of Prussia, PA: develop and validate statistical models and SAS programs to analyze, manage and interpret large scales of clinical data for new drug development. Develop and review SAP and clinical trial protocol; validate clinical trial reports and TLGs to support FDA submission. Req.: Master's degree/equiv. in Biostatistics, Statistics or related, strong skills in statistical analyses (linear regression analysis, logistic regression analysis) and statistical modeling using SAS tools and R. SAS Advanced Programmer Certificate. Send resume to TechData Service Company LLC, 700 American Ave., Suite 102, King of Prussia, PA 19406.
Statistical Programmer:
Work in King of Prussia. Provide statistical analyses support for R&D projs. Perform statistical analysis related to new drug development using advanced SAS/STATIMACRO/GRAPH SQL. Create customized programs for projects.
Min: MS in Biostatistics, Math, or related. Send Resume to: Techdata Service Company, LLC. 700 American Avenue, King of Prussia PA 19406
Senior Statistician (King of Prussia, PA):
Responsible for clinical trial design/planning relating to statistical analysis and reporting activities for Phase I/II/III clinical study projects; develop statistical analysis plans (SAP) & data specifications such as shells for tables/listings/figures (TLFs) and related database; review and study protocol by identifying issues/solutions related to statistical methodology and regulatory requirements; manage time lines and quality for all statistical deliverables; interact with medical writers in production of statistical and integrated clinical study reports; develop statistical modeling for statistical analysis, analysis datasets (ADS), TLFs setup utilizing SAS program; provide statistical consultation & support to clinical team by providing adequate information and summarized statistics; coordinate with clinician/CRO/PM to obtain clean and accurate data, validate datasets or derived datasets and review clinical study report for FDA submission. Master's degree in Statistics, Biostatistics, Math or related plus 1 year experience in job or as a statistician involving design, planning and statistical analysis of clinical trial with CRO or pharmaceutical company. Experience must include developing statistical modeling, clinical study design and observational study methodology using SAS programming.
Sr. Statistical Programmer (2 x openings in King of Prussia, PA): Provide advanced statistical analysis & SAS programming to support clinical research projects & FDA submission. Develop and validate SAS programs for analysis datasets and generation of TLFs. Review clinical study protocols and statistical analysis plan. Req: Master/ equiv in Statistics/Biostatistics/related; strong skills in clinical SAS programming, developing analysis datasets and specifications; proficiency with SAS /STAT /MACRO /GRAPH /SQL; SAS Advanced Programmer Certificate. Send resume to TechData Service Company LLC, 700 American Ave, Suite 102, King of Prussia, PA 19406.