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Clinical Research Site Recruitment Specialist

Company: Vitalief
Location: New Brunswick
Posted on: May 11, 2022

Job Description:

Job Description Why Vitalief? An exponentially growing, innovative Clinical Trial Solutions Company, Vitalief is committed to identifying talented and ambitious clinical research professionals to join our exceptional team as experts and members of our clients--- research efforts. Unlike a staffing agency, we provide solutions and support services to evolve clinical trials processes in this rapidly evolving industry and optimizing outcomes. Though none of this is possible without the drive and passion of those working on the trials, which can be you If you are interested in being part of a culture that includes: The ability to have a voice challenging the status quo with novel thinking Flexible work environment Transparency Investment in your career progression Variable incentive/reward system Encouraged and mentored by colleagues to achieve full potential Then we want to speak with you Note: This role is currently 100% remote, however, only candidates that live in New Jersey, the New York City area, and the Greater Philadelphia area will be considered for this position. This position is ideal path for someone that wants to eventually move into a Clinical Research Coordinator role. Responsibilities: Serves as the point person to work with investigators to determine if there is a sufficiently large pool of potential participants to meet recruitment targets. Assists the investigator and Research Study Manager with drafting a recruitment plan for each study through multiple methods including but not limited to ICD code EMR searches, AI based technology solutions such as Deep6, EPIC Slicer/Dicer and Clinical Research Data Warehouse searches. Following Institutional Review Board (IRB) approval uses Deep6 AI Cohort Builder to query the electronic medical record to generate a list of potential participants who appear to meet study eligibility criteria. Query and extract data from a variety of different sources to identify potential patients who match complex clinical trial inclusion/exclusion criteria of a particular study. Coordinates sponsor feasibility assessments. Works with the investigator and Research Study Manager to make sure that any study proposed has appropriate resources and clinical and hospital facility access to improve start-up time and success of studies. Works with Investigators and other members of the clinical research team to actively prescreen patients as potential research study participants for available trials. Collects and organizes patient data. Reviews data for quality and completeness based on established queries and refers patients to research team for additional screening and evaluation. Maintains a thorough understanding of assigned study inclusion/exclusion criteria and utilize these criteria to effectively assess potential participants. Tracks pre-screening/screen activities by trial in OnCore--. Evaluates and tracks the eligibility of patient queries for eligibility to assigned research studies. Required Skills: At least 6 to 12 months of experience (internships included) working in a corporate environment and/or within the pharmaceutical or healthcare industry (preferred). Bachelor---s degree required. Must be computer literate with proficiency and working knowledge of database and reporting tools such as Microsoft Word, Excel, PowerPoint, and REDCAP. Working knowledge of Clinical Trial Management Systems preferred. Must be detail oriented, have excellent organizational, communication and interpersonal skills. Self-accountable to high standards of professional excellence, be able to maximize resources and be resourceful, seeks and accepts personal and professional responsibility on a continued basis. Good communication skills, both oral and written are mandatory in order to clearly, effectively, and tactfully interact with faculty and potential patients (to enroll in a trial). Demonstrated ability to prioritize and manage multiple tasks. Ability to think logically and critically evaluate and solve problems. LI-DNI Powered by JazzHR IlIec4mfcw

Keywords: Vitalief, New Brunswick , Clinical Research Site Recruitment Specialist, Human Resources , New Brunswick, New Jersey

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