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Clinical Research Study Manager

Company: Vitalief
Location: New Brunswick
Posted on: May 4, 2022

Job Description:

Job Description Overview Vitalief is a fast growing, "best of breed" Clinical Trial Solutions Company. We are seeking a talented and ambitious Research Study Manager to join our exceptional team, that will serve as an expert clinical practitioner and member of the research team for our client. The primary purpose of the Research Study Manager is to establish workflows and processes to support high-quality clinical research activities. Our approach explores innovative ways of delivering services in a distributed model that can support both decentralized and centralized trials. Every trial is different and requires a solution that will optimize outcomes. 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, transparent and open communications, career pathing, and a variable incentive / reward system, then we want to speak with you Note: Work is 100% on-site in North-New Brunswick, New Jersey. Responsibilities: Serves as the primary liaison between our client and its affiliate sites as it relates to clinical research. Responsible for the supervision of day-to-day clinical research coordination operations as they relate to the Total Cancer Care Protocol. Supervision and assignment of assigned team. Ensures Clinical research processes are patient centered. Training and development of staff. Conducts Quality Assurance audits. Participates in Regulatory Compliance activities. Maintains knowledge of and participation in Performance Improvement (PI) activities. Works collaboratively with physician colleagues, nurses, nurse coordinators, pharmacy, reception staff, partnering staff and all members of our client's Research Services, Advanced Practice Nurses, appropriate hospital, and laboratory staff to ensure that services are coordinated and delivered to patients in a timely manner. Attends training programs, modules, workshops, and seminars sponsored by our client, disease-specific meetings, and meetings with the Principal Investigator, when directed by supervisor, to keep up to date on project objectives. Reviews all applicable guidelines and incorporates information into the daily workplace. Maintains SOCRA (Society of Clinical Research Associates) CCRP (Clinical Research Professional) or ACRP CCRC certification. Keeps abreast of all pertinent federal, state and client specific regulations, laws, and policies as they presently exist and as they change or are modified. Required Skills: Bachelor's Degree in a social science or related field. 3-5 years of oncology research experience required. 1-2 years of supervisory experience in a clinical research environment preferred. Supervision in a unionized environment preferred. Association of Clinical Research Professional (ACRP) certification or Society of Clinical Research Associates (CCRP) certification required. The ideal candidate will be detail oriented, have excellent organizational skills, be proficient in computer applications (Word, Excel, Oncore---), possess excellent communication and interpersonal skills, be able to maximize resources and be resourceful. Bilingual skills preferred. If interested in finding out more about opportunities with Vitalief, please contact: Glenn Murani Director of Talent Acquisition Vitalief Inc. (610) 209-1083 LI-DNI Powered by JazzHR 2J2kl6cksz

Keywords: Vitalief, New Brunswick , Clinical Research Study Manager, Healthcare , New Brunswick, New Jersey

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