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    Clinical Research Technician / Madison, Wi (On-Site)

    Fortrea
    2+ years
    Not Disclosed
    Remote, USA
    10 Nov. 6, 2024
    Job Description
    Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Job Title: Research Technician, Clinical Research
    Company: Fortrea
    Location: Madison, WI
    Employment Type: Full-Time, Office/Clinic-Based
    #LI-EC1

    About Fortrea:

    Fortrea is a leading global contract research organization (CRO) that provides clinical development, patient access, and technology solutions across over 20 therapeutic areas. We operate in more than 90 countries and partner with pharmaceutical, biotechnology, and medical device companies to advance drug and device development, improving patient outcomes worldwide.

    Position Overview:

    Fortrea is looking for a Research Technician to join our team in Madison, WI. As a Research Technician, you will interact directly with healthy volunteer participants in clinical trials while learning to read and interpret clinical research protocols. This role is ideal for individuals looking to make a meaningful impact in the field of clinical research, particularly in early-phase trials, by contributing to the safety, tolerability, and pharmacokinetics of new drugs.

    This is a full-time, office/clinic-based position with a mix of shifts, including morning, night, and weekend shifts.

    What You Will Do:

    As a Research Technician, you will provide direct care and support to clinical trial participants and assist in the execution of clinical research protocols. Key responsibilities include:

    • Clinical Care & Support:

      • Perform blood pressure, venipuncture, weight, pulse, respiratory rate, and temperature readings.
      • Prepare and record ECGs/Holters and assist with their processing.
      • Collect and process biological samples as specified in study protocols, ensuring proper distribution.
      • Monitor participants’ meals to ensure dietary compliance.
      • Assist with the preparation of rooms and medical equipment for study procedures.

    • Clinical Research Procedures:

      • Assist with screening procedures and maintain a clean, safe, and efficient study environment.
      • Respond to emergency situations in a manner consistent with clinical research standards.
      • Maintain accurate and timely documentation of clinical trial activities in electronic systems.

    • Team Collaboration:

      • Work in a fast-paced, team-oriented environment where collaboration is essential to ensure study timelines and protocols are strictly adhered to.
      • Adapt quickly to changing priorities and ensure quality control in all aspects of research.

    • Additional Duties:

      • Perform other duties as assigned to ensure smooth running of clinical trials.

    Qualifications:

    Required:

    • High School Diploma or equivalent.
    • EMT, Phlebotomy, CMA, or CNA certification preferred.
    • 1-2 years of clinical research or medical experience is preferred but not required. Recent graduates or candidates with healthcare experience are welcome to apply.

    Experience/Skills:

    • Comfort in a fast-paced, high-pressure environment, where strict adherence to protocols and timelines is critical.
    • Ability to adapt quickly to changing priorities and demands.
    • Strong teamwork and interpersonal skills to work closely with study participants and other team members.
    • Comfort with technology and electronic data collection systems.

    What You Will Get:

    • Comprehensive benefits package for regular, full-time employees working 20+ hours per week, including:
      • Medical, Dental, Vision, Life, STD/LTD (Multiple insurance carriers)
      • 401(K)
      • Paid Time Off (PTO)
      • Employee recognition awards
      • Opportunities to participate in Employee Resource Groups (ERGs)

    Why Fortrea?

    At Fortrea, you’ll be joining a global leader in clinical research, working alongside some of the world’s foremost pharmaceutical, biotechnology, and medical device companies. This is an opportunity to directly impact the development of new medical treatments and technologies that will improve the lives of patients around the world.

    Fortrea is an Equal Opportunity Employer:
    We are committed to diversity and inclusion in the workplace and do not tolerate discrimination of any kind. We encourage applicants from all backgrounds and experiences to apply.

    Application Deadline:
    Rolling applications until the position is filled.

    For more information about how we collect and store your personal data, please see our Privacy Statement.

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