Clinical Research Study Manager
Company: Vitalief Inc.
Location: New Brunswick
Posted on: May 13, 2022
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.
I f 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.
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
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
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
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
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.
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
Supervision in a unionized environment preferred.
Association of Clinical Research Professional (ACRP) certification
or Society of Clinical Research Associates (CCRP) certification
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:
Director of Talent Acquisition
Keywords: Vitalief Inc., New Brunswick , Clinical Research Study Manager, Executive , New Brunswick, New Jersey
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