Clinical Programmer jobs in Idaho

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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Clinical Research Assistant
  • Velocity Clinical Research, Inc.
  • Meridian, ID FULL_TIME
  • Overview

    Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.

     

    As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.

     

    Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.

     

    Summary:

    • The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.

    Responsibilities

    Role & Responsibilities:

    • Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs
    • Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
    • With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations
    • Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
    • Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
    • Enter source data into the sponsor's and/or vendor’s data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator
    • Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team
    • Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems and resolving queries under the direction of the Clinical Research Coordinator
    • Understand the informed consent process with emphasis on ensuring initial and ongoing consent of study subjects
    • Understand basic elements of regulatory documentation required to initiate, maintain and close a clinical research trial
    • Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person
    • Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
    • Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team
    • Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed
    • Prepare source document charts, copy and/or file medical records and study related documents as required.
    • Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.
    • Other duties as assigned

    Qualifications

    Education/Experience:

    • High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

    Required Licenses/Certifications:

    • Phlebotomy if applicable and required by state law
    • Intramuscular dose administration and preparation if applicable and required by state law

    Required Skills:

    • Demonstrated knowledge of medical terminology
    • Demonstrated ability to use the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
    • Understanding of verbal, written, and organizational skills
    • Demonstrated ability to work as a team player
    • Demonstrated ability to read, write, and speak English
    • Demonstrated ability to multi-task
    • Demonstrated ability to follow written guidelines
    • Demonstrated ability to be flexible/adapt as daily schedule may change rapidly

    Required Physical Abilities:

    • Sit or stand for long periods of time
    • Communicate in person and by a telephone
    • Limited walking required
    • Limited to lifting up to 30 pounds

    Velocity is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic. We are an E-Verify Employer in the United States.

     

  • 1 Month Ago

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Pascal Programmer
  • Procom Consultants Group
  • Idaho Falls, ID FULL_TIME
  • Company DescriptionProcom is a leading provider of professional IT services and staffing to businesses and governments in Canada.With revenues over $500 million, the Branham Group has recognized Proco...
  • 13 Days Ago

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Sheet Metal Layout Programmer
  • STEELHEAD METAL CORP
  • Nampa, ID FULL_TIME
  • Job Title: Sheet Metal Machine Layout/Programmer Location: Nampa, Idaho Company: Steelhead Metal Corp. About Us: Established in 1994, Steelhead Metal Corp is a leading supplier and manufacturer to the...
  • 1 Day Ago

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CNC Machine Operator and/or Programmer
  • Aerocet, Inc.
  • Priest River, ID FULL_TIME
  • Aerocet® is looking for a CNC Machine Operator and/or Programmer to program, set-up, operate, and maintain CNC Machine tools. Applicants will be 18 , with the ability to stand on concrete 10 hrs/day a...
  • 8 Days Ago

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210821 / Pascal Programmer
  • Procom Services
  • Idaho Falls, ID FULL_TIME
  • Company DescriptionProcom is a leading provider of professional IT services and staffing to businesses and governments in Canada.With revenues over $500 million, the Branham Group has recognized Proco...
  • 13 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

Idaho (/ˈaɪdəhoʊ/ (listen)) is a state in the northwestern region of the United States. It borders the state of Montana to the east and northeast, Wyoming to the east, Nevada and Utah to the south, and Washington and Oregon to the west. To the north, it shares a small portion of the Canadian border with the province of British Columbia. With a population of approximately 1.7 million and an area of 83,569 square miles (216,440 km2), Idaho is the 14th largest, the 12th least populous and the 7th least densely populated of the 50 U.S. states. The state's capital and largest city is Boise. Idaho p...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Programmer jobs
$59,536 to $75,490

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Here is an interview that CK Clinical conducted with one SAS Programmer working within the Pharmaceutical industry.
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Computer programmers write and test code that allows computer applications and software programs to function properly.
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While Clinical Trials Programmer exam includes topics from.
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