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Statistical programmer
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Katalyst Healthcares and Life Sciences New York, United StatesResponsibilities:A statistical programmer consultant provides timely support to the study team on all programming matters according to the project strategies. · Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal ...
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Statistical programmer
1 week ago
Katalyst HealthCares & Life Sciences New York, United StatesResponsibilities: A statistical programmer consultant provides timely support to the study team on all programming matters according to the project strategies. · Requirements will be identified according to a Statistical Analysis Plan and programming specifications using interna ...
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Senior Statistical Programmer
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Diverse Lynx New York, United StatesJob Title: Senior Statistical Programmer · Location: Groton CT, New York City, and Collegeville PA · Duration: Full-time only · Job Description : We are looking for an associate with at least 5+ years of experience for Sr Statistical programming position, having strong understa ...
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Manager, Statistical Programmer
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Takeda Pharmaceutical new york city, United StatesBy clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda'sPrivacy Notice and Terms of Use. I further attest that all information I submi ...
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Senior Statistical Programmer
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EG Life Sciences (now Eliassen Group) New Jersey, United StatesNO THIRD PARTY CANDIDATES · Eliassen is looking to add to our PK/PD FSP team, servicing a large Pharmaceutical client. · Detailed Job overview/ requirements · Ability to contribute to and lead standardization of processes for PKPD group including dataset creation, QC process, re ...
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Senior Statistical Programmer
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Statistical Programmer
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Statistical Programmer
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Source One Technical Solutions Parsippany, United StatesSource One is a consulting services company and we're currently looking for the following individual to work as a consultant to our direct client, a global pharmaceutical company in Parsippany, NJ. · Job Title: Statistical Programmer (Contractor) · Initial Duration: One year wit ...
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Statistical Programmer
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The Execu|Search Group Tarrytown, United StatesA recognized company in the Life Sciences industry is currently seeking a new Statistical Programmer to join their team in a Remote capacity. In this role, the Statistical Programmer will be responsible for providing timely support to the study team on all programming matters acc ...
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Statistical Programmer
1 week ago
Source One Technical Solutions Parsippany, United StatesSource One is a consulting services company and we're currently looking for the following individual to work as a consultant to our direct client, a global pharmaceutical company in Parsippany, NJ. · Job Title: Statistical Programmer (Contractor) · Initial Duration: One year with ...
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Statistical Programmer
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ShiftCode Analytics Parsippany, United StatesSTATISTICAL PROGRAMMER · 6+ MONTHS CONTRACT · PARSIPPANY, NEW JERSEY · HYBRID (2-3 DAYS/WEEK) · VISA- NO CPT/H1B · Manager-Statistical Programming, a hands-on with expert-level programmer in SAS and SQL, will lead in programming, managing and analyzing commercial administrati ...
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Statistical Programmer
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Katalyst Healthcares and Life Sciences Rahway, United StatesResponsibilities: Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies. · Provide statistical oversight to studies and assure adequate quality and consistency with project requireme ...
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Sr. Statistical Programmer
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Senior Statistical Programmer
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Katalyst Healthcares and Life Sciences South Plainfield, United StatesRoles & Resonsibilities: · We are looking for an associate with at least 5+ years of experience for Sr Statistical programming position, having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards. · SDTM/ADaM Model and IG. ...
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Sr. Statistical Programmer
1 week ago
Yoh Parsippany Troy Hills, NJ, United StatesYoh has an exciting, opportunity for a Sr. Statistical Programmer to join our rapidly growing life science manufacturing client based in Parsippany, NJ. · The Senior Statistical Programmer, an adept programmer proficient in SAS and SQL, will oversee programming, management, ...
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Principal Statistical Programmer
1 day ago
Regeneron Pharmaceuticals, Inc. Basking Ridge, United States Full timeThe Principal Statistical Programmer will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submiss ...
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Principal Statistical Programmer
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Katalyst HealthCares & Life Sciences Basking Ridge, United StatesResponsibilities: · Lead statistical programming activities as product lead for full development project or groups of projects in Oncology Therapeutics. · Attending multi-disciplinary team meetings, representing the statistical programming function. · Create or review and appr ...
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Principal Scientist- Statistical Programmer
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Merck Rahway, United States**Job Description** · This position focuses on strategic activities impacting late-stage development therapeutic area (TA) projects to the direct benefit of project teams and the Biostatistics organization. · The position is a key collaborator with internal and external stakehold ...
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Sr. Manager, Statistical Programmer
2 weeks ago
Yoh Parsippany Troy Hills, NJ, United StatesYoh has an exciting, opportunity for a Sr. Manager, Statistical Programming to join our rapidly growing life science manufacturing client based in Parsippany, NJ. · The Senior ManagerStatistical Programming, an adept programmer proficient in SAS and SQL, will oversee programm ...
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TechData Service Company LLC Basking Ridge, United StatesJob Description · Job DescriptionSr. Biostatistician · Responsibilities · At project level, ensures the study designs are scientifically sound, the efficacy and safety endpoints meets regulatory requirements. · Provide statistical support to Clinical Development Plan for multiple ...
Principal Statistical Programmer - New York, United States - IQVIA
Description
Location:
Homebased anywhere in the US Purpose:Experienced R programmers needed to provide technical expertise to develop process methodology for department to meet internal and external clients needs.
Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.Job Details:
Position:
Principal Statistical Programmer Home Based Min 4+ years of CRO/
Pharma Industry Therapeutic Areas:
Oncology // Immunology // IDV // EDCP
Key Skills:
Must have expertise of R programming as well as SAS Base, and good knowledge of SAS graph and SAS Macros.
Capable of implementing more advanced statistical procedures as per specifications provided by biostatistician. Must have excellent knowledge of CDISC standards (SDTM and ADaM) Thorough understanding of relational database components and theory. Excellent application development skills. Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results. Good understanding of ICH E6, ICH E3, ICH E8, ICH E9 and clinical research processes.Minimum of 4+ years of experience in Statistical Programming in pharmaceutical or medical devices industry Good verbal and written communication skills.
Ability to work on multiple projects, plan, organize and prioritize activities.Required Knowledge, Skills and Abilities:
Experience as technical team lead directly engaging clients and coordinating tasks within a programming team In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines? Knowledge of statistics, programming and/or clinical drug development process Advanced knowledge of R programmingBase SAS, SAS/STAT, SAS Graph and SAS Macro Language Should have experience with SDTM Implementation and ADaM implementation according to CDISC Standards.
Must have expertise in SAS/BASE, SAS/MACRO, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/ODS, SAS/SQL.Good organizational, interpersonal, leadership and communication skills Ability to independently?manage multiple tasks and projects Ability to delegate work to other members of the SP team Excellent accuracy and attention to detail Ability to delegate work to other members of the SP team [SPM] Exhibits routine and occasionally complex problem-solving skills Ability to lead teams and projects and capable of managing at a group level Recognizes when negotiating skills are needed and seeks assistance.
Ability to establish and maintain effective working relationships with co-workers, managers and clients.Responsibilities:
Perform, plan co-ordinate and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files? for internal and external clients and (iii) the programming? quality control checks for the source data and report the data issues periodically.
Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department, for complex studies.
Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines.
Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables. Use and promote the use of established standards, SOP and best practices. Provide training and mentoring to SP team members and Statistical Programming department staff.MINIMUM REQUIRED EDUCATION AND EXPERIENCE:
Bachelor's degree from reputable university preferably in science/ mathematics related fields IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world.
Learn more at We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.IQVIAs ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.
The potential base pay range for this role, when annualized, is $119, $203, The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).
Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
SummaryLocation:
Durham, North Carolina, United States of America; Norfolk, VA; Trenton, NJ; Chicago, IL; Seattle , WA; San Francisco , CA; Miami, FL; Phoenix, AZ; Charlotte, NC; Overland Park, KS; Jacksonville, FL; Los Angeles, CA; Washington, DC; Atlanta, GA; Boston, MA; Nashville, TN; Dallas, TX; Houston, TX; Philadelphia, PA; Baltimore, MD; New York City, New York, United States; Austin, TXType: Full time