Jobs
>
Princeton

    Principal Statistical Programmer - Princeton, United States - WCG Clinical

    WCG Clinical
    WCG Clinical Princeton, United States

    2 weeks ago

    Default job background
    Description

    Principal Statistical Programmer (Remote)

    General Information

    Location: Princeton, NJ, Remote

    Organization: Statistics Collaborative

    Job Type: Full Time - Regular

    Description and Requirements

    ABOUT WCG : WCG's clinical solutions are built on a foundation of best-in-class clinical services companies. We deliver transformational solutions that stimulate growth, foster compliance, and maximize efficiency for those performing clinical trials. WCG is proud to serve individuals on the frontlines of science and medicine, and the organizations striving to develop new products and therapies to improve the quality of human health. It is our role to empower them to accelerate advancement, while ensuring the risks of progress never outweigh the value of human life.

    WHY WE LOVE WCG : At WCG, our employees are our most valuable asset, and as with all our assets, we invest in them with an eye toward future success. We provide each eligible employee with a comprehensive set of benefits designed to protect their personal and financial health to help make the most of their future.

    • Comprehensive Benefits package - Health, Dental, Vision, Life Disability, 401k with match, and flexible spending accounts
    • Employee Assistance Programs and additional work/life resources
    • Referral Bonuses and Tuition Reimbursement
    • Flexible PTO
    • Volunteer Time Off to benefit the community
    • Opportunities for career development with on-the-job training, certification assistance, and continuing education reimbursement

    Expected annual base salary range: $124,800 to $152,000

    GPS level: P4

    JOB SUMMARY: A Principal Statistical Programmer will (a) mentor and oversee the statistical programming tasks by more junior staff, (b) develop approaches to improve programming efficiency and product quality, and (c) co-lead biostatistical projects. A Principal Statistical Programmer will be proficient in writing efficient programs and will be able to guide others in programming.

    ESSENTIAL DUTIES/RESPONSIBILITIES : To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or ability required.

    • Program and perform quality control of complex programs in Scientific Review, including programming of complex SDTM, ADaM, and summary TFLs.
    • Lead programming of biostatistical projects with minimal oversight from senior staff.
    • Utilize data standards and regulatory conventions such as CDISC, when needed.
    • Work with project management on project budgets, including estimating hours for programming tasks, understanding the impact of these estimates on the budget, and being aware of project scope.
    • Review statistical analysis plans, protocols, charters, or other study documents and assist in the design of statistical data displays.
    • Assist in developing, validating, and coordinating the administration of in-house macros.
    • Share best coding practices to improve efficiency and quality of Scientific Review deliveries.
    • Serve as mentor for less experienced programmers.
    • Lead SAS training sessions for new employees and assist in maintaining and testing SAS software.
    • Stay up-to-date on current advances in statistical programming.
    • Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.

    EDUCATION REQUIREMENTS: BS or BA required

    QUALIFICATIONS/EXPERIENCE:

    • At least five years of post-Bachelor's experience in Clinical SAS Programming, analyzing data, working in a team environment, and participating in managing projects.
    • Extensive SAS programming in a clinical trial setting and with regulatory conventions.
    • Attention to detail, accuracy, initiative, and excellent communication skills are essential, as well as the ability to juggle several complex tasks simultaneously.

    TRAVEL REQUIREMENTS:

    ☒0% – 5%

    ☐5% - 10%

    ☐10% - 20%

    ☐20% - 50%

    ☐>50%

    Physical and Sensory Requirements: The physical and sensory requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be offered to individuals with disabilities to assist in performing the essential functions of the position. Work activities involve light to moderate physical effort (for example, sitting in one place for extended periods of time, standing, walking, bending, lifting lightweight objects, intermittent to sustained periods of keyboarding). Majority of time is spent in a seated position with frequent opportunity to move about at will. Activities require a variety of easy muscle movements. Work activities involve a frequent need to concentrate on a variety of sensory inputs for moderate to lengthy durations at a time requiring diligence and attention to interpret effectively. There will be a need to attend to single or simultaneous tasks where accuracy of details is important. The need for detailed and precise work is high.

    #LI-Remote

    WCG is proud to be an equal opportunity employer – Qualified applicants will receive consideration for employment without regard to race, color, national origin or ancestry, religion or creed, sex, sexual orientation, gender identity, age, marital status, disability, genetic information, citizenship, veteran status, reprisal or any other legally recognized basis or status protected by federal, state or local law.



  • TK-CHAIN LLC Princeton, United States

    **Minimum Requirements** | **Role Responsibilities**: · - Expertise in extracting, manipulating, summarizing, analyzing, and presenting data using SAS procedures · - Expertise in SAS/MACRO, SQL, and SAS/BASE procedures · - Expertise/experience in use of SAS/GRAPH and Statistical ...


  • WCG Princeton, United States

    **Description and Requirements**: · **ABOUT WCG**: WCG's clinical solutions are built on a foundation of best-in-class clinical services companies. We deliver transformational solutions that stimulate growth, foster compliance, and maximize efficiency for those performing clinica ...


  • TK-CHAIN LLC Princeton, United States

    Provide lead statistical programming support in the project specific programming of CDISC datasets (SDTM, ADaM), analysis outputs (tables, listings, figures), and ad hoc reports of all complexities. Provide leadership in project management of trials across several therapeutic are ...


  • TK-CHAIN LLC Princeton, United States

    Job Description · Job Description · Minimum Requirements | Role Responsibilities · Expertise in extracting, manipulating, summarizing, analyzing, and presenting data using SAS procedures · Expertise in SAS/MACRO, SQL, and SAS/BASE procedures · Expertise/experience in use of SAS/G ...


  • Takeda Pharmaceutical Trenton, United States Full time

    By 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 subm ...


  • TK-CHAIN LLC Princeton, United States

    Job Description · Job DescriptionProvide lead statistical programming support in the project specific programming of CDISC datasets (SDTM, ADaM), analysis outputs (tables, listings, figures), and ad hoc reports of all complexities. Provide leadership in project management of tria ...


  • Katalyst Healthcares and Life Sciences Plainsboro, United States

    Responsibilities: Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.). · Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies. · ...


  • System One Trenton, United States

    Job Title: · Statistical Programmer, RWE · Location: · Parsippany, NJ · Hours/Schedule: · 8am-4pm, or 9am-5pm M-F · Type: · 12 month contract · Overview · Our partner, a Domestic Pharmaceutical company in New Jersey, is currently seeking to hire a Statistical Programmer(RWE) ...


  • Wizsolution Plainsboro, United States

    Job Description · Job DescriptionJob Description · Company Descriptions: · Wizsolution is located in Princeton NJ, which is a leader in pharmaceutical recruitment and staffing. Our goal is to provide effective solutions for fulfilling your career potential. The mission of our com ...


  • Katalyst Healthcares and Life Sciences Rahway, United States

    Responsibilities: 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 ...


  • Everest Clinical Research Trenton, United States

    Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies ...


  • 5PY US Quintiles, Inc. Trenton, United States

    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 solution ...


  • Takeda Pharmaceutical Company Ltd Trenton, United States

    By 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 Takedas Privacy Notice and Terms of Use. I further attest that all information I submit ...


  • EG Life Sciences Trenton, United States

    NO 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 ...


  • Katalyst Healthcares and Life Sciences South Plainfield, United States

    Roles & 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. ...


  • Katalyst HealthCares & Life Sciences Basking Ridge, United States

    Responsibilities: · 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 ...


  • Regeneron Pharmaceuticals, Inc. Basking Ridge, United States Full time

    The 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 ...


  • 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 ...


  • TechData Service Company LLC Basking Ridge, United States

    Job 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 ...


  • Merck Rahway, United States

    **Job Description** · In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodolog ...