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    Mental Health Research Recruiter - Newark, United States - Vitalief Inc.

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    Description

    WHY VITALIEF?

    Vitalief was formed to address any concerns the clinical trial industry is facing today. We are expanding our footprint rapidly as a value-added, innovative Research and Clinical Trial Consulting Company. As a result, we are seeking talented and enthusiastic Clinical Research professionals to join our exceptional team (as full-time, fully benefited employees) to support our clients successful planning and execution of research and clinical trials.

    Reasons to work for Vitalief:

    • can actively contribute to our clients mission of advancing scientific discoveries that have the potential to change patients' lives for the better.
    • impact clinical research in various therapeutic areas, including oncology, and improve outcomes for diverse populations.
    • PEOPLE FIRST culture prioritizes personal and professional growth for all Vitalief employees.
    • give everyone a seat at the table we encourage innovation.
    • committed to our employees you are encouraged and mentored by the talented Vitalief team to achieve full potential.
    • balance that includes 20 PTO (Paid Time Off) days plus 9 paid Holidays annually.
    • benefits include Company paid life insurance and short / long term disability coverage; 401K retirement program; Robust healthcare plans to choose from.

    Salary Range: $70,000 to $83,000 annually depending on experience level.

    Work Location: office is based in Newark, NJ; however, the job will require 20% local travel to different communities across Newark, New Brunswick and Piscataway NJ areas.

    Responsibilities:

    Under the direction of the Director of the Center for Genomics of Psychiatric Health & Addiction (CGPHA), the interviewer responsible for the conduct of representative studies of persons with psychiatric illness and those with no mental health diagnosis, including recruitment and enrollment of participants from diverse ethnic communities through administration of screening and clinical diagnostic instruments and surveys. Current funded research studies focus on the enrollment of minorities under-represented in research, in particular those of Latinx and African ancestry.

    • as part of the enrollment team to conducting diagnostic validity and reliability standards for the use of diagnostic instruments including the DIPAD.
    • semi-structured diagnostic interviews relevant to ongoing investigatory activities of the CGPHA.
    • follows research protocols including administering study consent, study diagnostic instruments, providing compensation to participants and recording all data in the study database.
    • with instructing and training of lower-level study raters, recruiters and phlebotomists to develop the skills necessary to perform the required functions.
    • all data in the study database and performs the necessary Q/C for data in the study database.
    • in and leads both on-site and off-site community engagement and study recruitment activities and will maintain and/or develop networking and community relationships.
    • recruitment activities to maximize access to potential participants, which may involve irregular work scheduling to match community needs and availability, requiring occasional evening and weekend work and off-site local travel.
    • abreast of all pertinent federal, state and client compliance standards.

    Required Skills:

    • Degree in a relevant science (i.e., psychology, public health) plus 2 years of related experience.
    • in mental health and interacting with and interviewing patients with Schizophrenia, bipolar or OCD in a clinical setting OR for a clinical study.
    • (English/Spanish) speaking.
    • interacting with the diverse ethnic communities in New Jersey.
    • being willing to accommodate a flexible work schedule and have access to personal transportation frequently commuting to different communities across Newark, New Brunswick and Piscataway NJ areas to conduct field activities and recruit subjects, then schedule time in office to interview subjects which will require occasional evening and weekend work.
    • communication skills, both oral and written are mandatory.
    • organizational and interpersonal skills.
    • ability to prioritize and manage multiple tasks.
    • to attend to detail, think logically and critically evaluate and solve problems.

    Preferred Skills:

    • community relationships and/or ties with groups who face additional barriers accessing healthcare and social services, and/or have demonstrated such expertise in a similar setting in past professional activities.
    • Research Experience
    • certification, or willingness to take phlebotomy training course.
    • and/or MCHES certification.

    PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Ability to travel to local sites in Newark NJ and surrounding areas. 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.



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