Research Coordinator

Req #: 0000251168 Category: Clerical / Administrative Status: Full-Time Shift: Day Facility: Cooperman Barnabas Medical Center Department: Research Department Pay Range: $57,000.00 - $65,000.00 per year Location: 94 Old Short Hills Road, Livingston, NJ 07039 Job Title: Research Coordinator Location: Cooperman Barnabas Medical Ctr Department Name: Research Department Req #: 0000251168 Status: Salaried Shift: Day Pay Range: $57,000.00 - $65,000.00 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. Job Overview As a member of the CBMC Clinical Research office, the Research Coordinator serves as the primary Study Coordinator managing clinical trials, registries, and investigator-initiated projects from pre-activation through study close-out. Works autonomously and with limited oversight to execute end-to-end operational activities, including participant recruitment, safety reporting, specimen processing, and regulatory compliance. Collaborates directly with Principal Investigators and the Clinical Research Office to ensure data integrity, financial accuracy, and audit-ready documentation. Service Line/Therapeutic Area Assignment: Stroke Research (Assignments may be changed at any time to meet the needs of the department) Qualifications Required: Bachelor degree or equivalent in health science, business administration, health care administration or related discipline Proficiency in using various Microsoft Office applications such as World, Excel, Access, Power Point and Outlook Effective oral, written, communication, interpersonal skills Ability to interface effectively with all levels of management and must work and communicate effectively with both internal and external partners Ability to work and make decisions independently Time management skills and ability to multi task Strong understanding and knowledge base of coordination requirements associated with clinical/research trials Preferred Clinical research and/or patient care experience in the assigned service line/therapeutic area (Preferred) Minimum of two years of progressively responsible related experience coordinating clinical/research trials studies (Preferred) CITI Training (Preferred) Scheduling Requirements Shift-7:00am-3:00pm Monday -Friday Full time-Day Essential Functions Functions as a Study Coordinator on Investigator-Initiated projects, registries, and clinical trials. Maintains thorough knowledge of research studies including, but not limited to, study rationale & objectives, study subjects, and schedule of events Supports participant recruitment, screening, enrollment, and retention efforts to meet study accrual goals Facilitates end-to-end clinical trial operations across all study visits, pre-activation setups, participant follow-ups, and study close-out procedures Initiates and continues regular contact with patients; encourages visit reminders and compliance to research; ensuring contact with patients and their families is courteous, effective, professional and cooperative Maintains accurate, timely, and audit-ready source documentation in accordance with GCP and ALCOA principles Documents and reports informed consent, adverse events, serious adverse events, protocol deviations, and safety concerns in accordance with Sponsor, IRB, FDA, and institutional requirements Supports sponsor monitoring visits, internal audits, and regulatory inspections. Collaborates with the Principal Investigators to oversee the conduct of assigned studies and participates in research program development and planning Prepares, submits, and archives IRB applications, amendments, continuing reviews, deviations, study closure documentations, and other regulatory and essential documents. Utilizes electronic data capture systems, clinical trial management systems, and electronic medical records to maintain accurate study documentation and data integrity. Assists investigators with data compilation, abstracts, manuscripts, presentations, and publication- related activities Processes, tracks, stores, and ships biological specimens per protocol and institutional requirements Develops and maintains budgets, financial tracking logs, invoices, patient stipends, and other finance related documents Attends and maintains appropriate trainings including but not limited to, Good Clinical Practice, Conflicts of Interests, Biomedical Research, Biological Substances processing and shipping, HIPAA, and Ethics/IRB Collaborates with various personnel and staff to execute research activities and provides general or protocol specific in-service/trainings, as applicable Acts as a liaison for the Clinical Research Office to all assigned service lines/ therapeutic areas Collaborates with the Clinical Research Office to support, coordinate, and advance departmental initiatives Conducts all other duties and responsibilities as assigned Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. Benefits And Perks At RWJBarnabas Health, our employees are at the heart of everything we do. Driven by our Total Wellbeing promise, our market-competitive offerings include comprehensive benefits and resources to support our employees’ physical, emotional, financial, personal, career, and community wellbeing. These benefits and resources include, but are not limited to: Paid Time Off including Vacation, Holidays, and Sick Time Retirement Plans Medical and Prescription Drug Insurance Dental and Vision Insurance Disability and Life Insurance Paid Parental Leave Tuition Reimbursement Student Loan Planning Support Flexible Spending Accounts Wellness Programs Voluntary Benefits (e.g., Pet Insurance) Community and Volunteer Opportunities Discounts Through our Partners such as NJ Devils, NJ PAC, and Verizon ….and more! Choosing RWJBarnabas Health! RWJBarnabas Health is the premier health care destination providing patient-centered, high-quality academic medicine in a compassionate and equitable manner, while delivering a best-in-class work experience to every member of the team. We honor and appreciate the privilege of creating and sustaining healthier communities, one person and one community at a time. As the leading academic health system in New Jersey, we advance innovative strategies in high-quality patient care, education, and research to address both the clinical and social determinants of health. RWJBarnabas Health aims to truly make a unique impact in local communities throughout New Jersey. From vastly improving the health of local residents to creating educational and career opportunities, this combination greatly benefits the state. We understand the growing and evolving needs of residents in New Jersey—whether that be enhancing the coordination for treating complex health conditions or improving community health through local programs and education. At RWJBarnabas Health, our market-competitive Total Rewards package provides comprehensive benefits and resources to support our employees physical, emotional, social, and financial health. Paid Time Off (PTO) Medical and Prescription Drug Insurance Dental and Vision Insurance Retirement Plans Short & Long Term Disability Life & Accidental Death Insurance Tuition Reimbursement Health Care/Dependent Care Flexible Spending Accounts Wellness Programs Voluntary Benefits (e.g., Pet Insurance) Discounts Through our Partners such as NJ Devils, NJ PAC, Verizon, and more! RWJBarnabas Health is an Equal Opportunity Employer #J-18808-Ljbffr