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    Clinical Research Specialist II - Boise, United States - Idaho State Job Bank

    Idaho State Job Bank
    Idaho State Job Bank Boise, United States

    1 week ago

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    Clinical Research Specialist II
    • Laminar, Inc.
    at J&J Family of Companies in Boise, Idaho, United States Job Description Clinical Research Specialist II
    • Laminar, Inc W Description Laminar, part of the Johnson & Johnson family of Medical Device companies, is current recruiting for a Clinical Research Specialist II .
    The preferred location for this role is within the Western half of the United States but remote options anywhere within the US will be considered on a case by case basis. About Johnson & Johnson At Johnson & Johnson, we believe health is everything.

    Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.

    Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

    Learn more at This Clinical Research Specialist will be responsible for supporting one or more clinical trials within the Clinical Affairs Department while fostering, productive relationships with colleagues across the organization.

    Duties and Responsibilities Serves as a Clinical Research Specialist within the Clinical Affairs Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones.

    May Participate in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the good clinical practices, applicable legislation and Company Standard Operating Procedures.

    May serve as the primary contact for clinical trial sites (e.g. site management). Assists in the development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports). Supports trial registration (e.g. from study initiation through posting of results and support publications as needed. May coordinate and complete ordering, tracking, and accountability of investigational devices and trial materials. Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel. May coordinate the development and execution of Investigator agreements and trial payments. Assists in clinical data review to prepare data for statistical analyses and publications. May perform monitoring activ To view full details and how to apply, please login or create a Job Seeker account
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