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    Clinical Research Coordinator - New Brunswick, United States - Vitalief

    Vitalief
    Vitalief New Brunswick, United States

    2 weeks ago

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    Description

    Job Description

    Job Description

    WHY VITALIEF?

    Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic. Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions.

    Reasons to Work for Vitalief:

    • Our PEOPLE FIRST culture prioritizes personal and professional growth for all Vitalief employees.
    • We give everyone a seat at the table – we encourage innovation.
    • We're committed to our employees – you are encouraged and mentored by the talented Vitalief team to achieve full potential.
    • "Life/Work" balance that includes 20 PTO (Paid Time Off) days plus 9 paid Holidays annually.
    • Other benefits include Company paid life insurance and short / long term disability coverage; 401K retirement program; Robust healthcare plans to choose from.

    Salary Range: $60,000 to $70,000 annually

    Work Location: Work is 5 days per week on-site in New Brunswick, NJ.

    Job Responsibilities:

    • Under the direct supervision of the Nurse Manager of Clinical Research Center (CRC), you will be responsible for performing a wide variety of tasks to ensure successful Oncology related clinical trials.
    • Manage eligibility check lists, perform patient screening/consenting (informed consent), patient activation and managing patient care (patient retention).
    • Assist with monitoring patient visits.
    • Track deviations and documenting SAEs (serious adverse events).
    • Ship specimens to central labs or research labs.
    • Track data queries and prepare data for an upcoming audit.
    • Work collaboratively with all team members (i.e., physicians, nurses, hospital, and laboratory staff) to ensure that services are coordinated and delivered to patients in a timely manner.

    Required Skills:

    • Minimum of 1 to 2 years of experience in Clinical Research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance and data management.
    • Bachelor's Degree required.
    • Any experience in Oncology and/or working on complex clinical trials is a plus.
    • Ability to work on 12 to 15 concurrent trials – must have strong organizational and prioritization skills.
    • The keys to success in this role are your ability to demonstrate your versatility, "can do" attitude, and adaptability.
    • Considerable understanding of Good Clinical Practice (GCP) guidelines.
    • Experience in preparation of documents for submission to the Institutional Review Board (IRB), continuing reviews, and submission of amendments and modifications.
    • Experience ensuring Serious Adverse Events (SAEs) are completed and reported to the QA Manager and sponsor, if necessary, within reporting deadlines outlined in the protocol.
    • Any exposure to EPIC (Electronic Health Records system) and/or OnCore (Clinical Trials Management System) is a plus.

    PHYSICAL DEMANDS: Standing, sitting, walking, talking, hearing, and visual perception. Lifting up to 25lbs.

    IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that requires all on-site resources such as prospective Vitalief consultants to provide proof that they are fully vaccinated for Covid-19; inoculated annually for Influenza; and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.

    #LI-DNI

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