Clinical Programmer jobs in New Jersey

Clinical Programmer evaluates, develops, and maintains clinical database and analyzes clinical data. Codes, tests and documents databases. Being a Clinical Programmer performs data validation and develops algorithms for data management, typically using SAS programming language. May require a bachelor's degree. Additionally, Clinical Programmer typically reports to a supervisor or manager. The Clinical Programmer works on projects/matters of limited complexity in a support role. Work is closely managed. To be a Clinical Programmer typically requires 0-2 years of related experience. (Copyright 2024 Salary.com)

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Principal Statistical Programmer
  • Everest Clinical Research
  • Bridgewater, NJ FULL_TIME
  • 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 and work with many of the most advanced drugs, biologics, and medical devices in development today.

    Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater, New Jersey, USA, Taipei, Taiwan, and Shanghai (Pudong Zhangjiang New District), China.

    Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.

    Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest.

    To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Principal Statistical Programmers for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.

    Key Accountabilities:

    • Lead projects with higher level of complexity/challenges/difficulties. Lead efforts to resolve complex statistical programming issues or problems.
    • Perform a leadership role in statistical programming projects by coordinating study team(s), overseeing timelines, assigning and following up on programming tasks, interacting with clients, and ensuring quality of programming deliverables.
    • Assist statistical programming management in properly planning and allocating resources based on timelines, statistical programmers’ skills and expertise, as well as availability.
    • Participate in developing and maintaining clinical trial data and statistical programming standards to ensure the company standards are up to date and in line with pharmaceutical industry standards, conventions, and regulatory requirements.
    • Perform hands on primary statistical programming and validation programming on assigned projects including but not limited to phase I – IV clinical trials, integrated clinical summaries, responses to requests from regulatory agencies, publication support, data explorations, data monitoring committee meetings, etc.
    • Create SDTM mapping specifications and ADaM data specifications. Perform quality control (QC) review of these documents prepared by others.
    • Create SDTM and ADaM define.xml files. Perform QC review of these files prepared by others.
    • Perform 3rd level QC review on programming deliverables before their release to the clients.
    • Perform QC review/assessment on regulatory submission programming documents, datasets, tables/listings/graphs (TLGs), and computer programs, etc.
    • May lead programming efforts for drug development programs or for assigned client clusters.
    • Provide training, mentorship, and technical guidance to less experienced Statistical Programmers or Biostatisticians who perform statistical programming.
    • Monitor the compliance and adherence to the established data and programming standards, and statistical programming governing documents.
    • May represent the company in interactions with clinical trial sponsors with regard to statistical programming projects and relevant businesses.
    • Participate in the development of statistical programming policies, SOPs, guidelines, and good working practices.
    • Participate in statistical programming project bidding or bid defense meetings.
    • Work with document management specialists/archivists to plan and perform archival of the statistical programming datasets, outputs, documents, and final programs upon the completion of the assigned projects. Perform transfer of the archived files to the clinical trial sponsors.

    Qualifications and Experience:

    • M.Sc., M.A. or higher degree in Statistics, Biostatistics, Computer Science, or relevant fields.
    • 10 (M.Sc., M.A.)/9 (Ph.D.) years’ related experience.
    • An in-depth knowledge of clinical trial data processing and manipulation, hands on statistical programming and analysis, requirements for assembling and presenting trial results to regulatory agencies. Knowledge of industry standards on how clinical trial data are structured, stored, analyzed, and presented. Knowledge of clinical trial regulatory and ICH requirements.
    • Must demonstrate ability to effectively plan, control, and carry on tasks in SAS programming, statistical analysis, and submission of trial data and results to regulatory agencies. Must possess in-depth level understanding of the concept of standardization in data, programming, and statistical reporting of trial results, and its implication to the relevant functions and operations. Must have sound technical judgment and experience in process design and implementation in relevant areas. Strong leadership and drive to achieve goals will be required.

    To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.ecrscorp.com

    We thank all interested applicants, however, only those selected for an interview will be contacted.

    Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.


    Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

    The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c)

  • 22 Days Ago

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Clinical Programmer
  • Katalyst Healthcares & Life Sciences
  • West Milford, NJ FULL_TIME
  • Company DescriptionKatalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.We have ...
  • 14 Days Ago

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Clinical Programmer Analyst
  • System One
  • Nutley, NJ CONTRACTOR
  • Job Title: Clinical Programmer Analyst Location: Remote - Must be US Based Compensation: $55.00- $60.00 Type: 12 month Contract - W2 only - Please not agencies Responsibilities Senior Rave Programmer ...
  • Just Posted

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Clinical Programmer Analyst
  • Zenith LifeScience LLC
  • Nutley, NJ CONTRACTOR
  • Accountable for developing programs to create SDTM for clinical trials for delivery to different internal groups and for submission to the regulatory authorities. Perform CRF annotation, specification...
  • 4 Days Ago

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Clinical SAS Programmer
  • Katalyst Healthcares & Life Sciences
  • Princeton, NJ CONTRACTOR
  • Responsibilities: Performing data manipulation, analysis, and reporting of clinical trial data, both safety and (ISS/Client), utilizing SAS programming. Generating and validating SDTM and ADaM dataset...
  • 10 Days Ago

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Clinical SAS Programmer
  • Katalyst Healthcares & Life Sciences
  • South Plainfield, NJ CONTRACTOR
  • Responsibilities: Develop, validate, and maintain SAS programs for clinical data analysis, reporting, and submission in adherence to CDISC standards, regulatory guidelines, and company SOPs. Lead the ...
  • 10 Days Ago

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Clinical Programmer Analyst
  • Zenith LifeScience
  • Nutley, NJ
  • • Senior Rave Programmer Responsible for designing the eCRF in leading EDC systems in Rave • Technical expertise, techni...
  • 3/29/2024 12:00:00 AM

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Senior Clinical Programmer Analyst - Remote
  • Maxis Clinical Sciences LLC
  • Nutley, NJ
  • Description: Remote Qualifications " Minimum 10 years of relevant work experience to include data management and/or data...
  • 3/29/2024 12:00:00 AM

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Senior Clinical Programmer Analyst
  • Tandym Group
  • Nutley, NJ
  • A pharmaceutical company in New Jersey is currently seeking a new Senior Clinical Programmer Analyst for a great remote ...
  • 3/28/2024 12:00:00 AM

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Senior Clinical Programmer Analyst
  • Infotech Spectrum Inc,
  • Nutley, NJ
  • Job Title: Senior Clinical Programmer Analyst Location: Nutley, NJ ( Remote, Consultant need to be in USA) Duration: Lon...
  • 3/28/2024 12:00:00 AM

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Clinical Programmer - Part-time (Remote)
  • ASRC Federal Holding Company
  • Greenbelt, MD
  • Job Description ASRC Federal proudly supports the NIH National Cancer Research and is seeking aClinical Programmerto sup...
  • 3/28/2024 12:00:00 AM

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Senior Clinical Programmer Analyst (100% Remote role)
  • Maxis Clinical Sciences
  • Nutley, NJ
  • Job Description Job Description SAS Programmer Analyst Can be 100% remote We need someone with SAS programming skills wi...
  • 3/28/2024 12:00:00 AM

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Director Clinical Development
  • Green Key Resources
  • Princeton, NJ
  • Must be available to come onsite 2x a week Responsibilities: • Provide scientific and clinical expertise to support the ...
  • 3/28/2024 12:00:00 AM

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SVP, Clinical Development
  • C4 Therapeutics Inc
  • Watertown, MA
  • Job Description Job Description Our Opportunity: C4 Therapeutics is seeking an experienced Oncologist to lead the Clinic...
  • 3/26/2024 12:00:00 AM

New Jersey is bordered on the north and northeast by New York (parts of which are across the Hudson River, Upper New York Bay, the Kill Van Kull, Newark Bay, and the Arthur Kill); on the east by the Atlantic Ocean; on the southwest by Delaware across Delaware Bay; and on the west by Pennsylvania across the Delaware River. New Jersey is often broadly divided into three geographic regions: North Jersey, Central Jersey, and South Jersey. Some New Jersey residents do not consider Central Jersey a region in its own right, but others believe it is a separate geographic and cultural area from the Nor...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Programmer jobs
$70,593 to $89,511

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While Clinical Trials Programmer exam includes topics from.
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