About this opportunity
RWJBarnabas Health lists this Manager opportunity in elizabeth, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Job Title: Manager
Location: CANCER CENTER
Department Name: Cancer Center
Req #
Status: Salaried
Shift: Day
Pay Range: $78,400.00 - $98,000.00 per year
Pay Transparency:
The above reflects the anticipated annual salary range for this position if hired to work in New Jersey.
The compensation offered to the candidate selected for the position will depend on several factors, including the candidate's educational background, skills and professional experience.
Research Manager – RWJBarnabas Health
At RWJBarnabas Health, the Research Manager for Oncology Services plays a critical role in patient care and operational excellence. Operating with a high level of independence, they perform complex clinical research oversight and trial management according to strict medical, legal, and professional Good Clinical Practice standards. They are responsible for exercising professional judgment during protocol evaluations, ensuring accurate regulatory documentation, delivering trial-specific compliance, and maintaining seamless workflow collaboration within the multidisciplinary oncology department.
A typical day for a Research Manager may include:
Prepares operational plans for oncology clinical trials, clearly explains the process, and coordinates study activation through closeout procedures
Operates clinical trial management systems, electronic health records, computers, and database applications necessary to ensure a safe and accurate tracking and monitoring procedure
Assist physicians and principal investigators during study selection and protocol implementation by managing recruitment, screening, or enrollment activities
Sets up regulatory binders and other essential files following human subject protection guidelines, handles contracts negotiation, and reviews budgets to assist with fiscal management
Calibrates, maintains, and adjusts research quality metrics, and reports protocol deviations, adverse events, or other problems immediately to the appropriate support or departmental leadership
Monitors and calls out trial data metrics, alerting the healthcare team immediately to any changes in patient condition or compliance issues
Utilizes research software and documentation systems to enter accurately identified and verified records of trial participants, and retrieves old laboratory or clinical reports when necessary
Demonstrates working knowledge of research protocols including IRB submissions, continuing reviews, safety, and audit preparation techniques
Collaborates professionally in an administrative or clinical research environment, working in close cooperation with physicians, advanced practice providers, and other technical staff
Demonstrates initiative, flexibility, and the ability to assume multi-task duties and function under significant time pressures
This role might be for you if:
You enjoy working as a team player and assisting those in need
Patient safety, accurate drug evaluation, and delivering high-quality pharmaceutical care are your top priorities
You enjoy working collaboratively with providers, nurses, and interdisciplinary care teams
You utilize a proactive approach and anticipate needs
Demonstrate respect and appreciation for each person regardless of that person’s background, race, gender, religion, disability or sexual orientation.
Continuous learning, inventory awareness, and operational efficiency motivate you
Creating a positive, reassuring, and legally compliant patient experience is central to your approach
To be considered for this Research Manager opportunity:
Graduate with a Bachelor's degree in a relevant field; a Master's degree is highly preferred
Problem-solving, critical thinking, decisive judgment, collaboration, and the ability to work with minimal supervision
Minimum of 3 years of managerial experience leading clinical research coordinators or specialists
Extensive experience managing oncology clinical trials from study activation through to closeout
Solid background in fiscal management, budget development, and contract negotiation for research protocols
Comprehensive knowledge of FDA regulations, ICH-GCP guidelines, IRB processes, and human subject protections
Proficiency working with clinical trial management systems (CTMS) and electronic medical records (EMR)
Certification through a recognized clinical trials professional organization (SoCRA or ACRP) is required
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Worksite address
elizabeth, NJ, 07215, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.