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Donor Research Coordinator jobs in New Jersey

Donor Research Coordinator identifies potential donors and evaluates their interests and capacity to give to the organization. Conducts research and prospecting to locate individuals aligning with the organization's values and mission. Being a Donor Research Coordinator analyzes data for trends and creates donor profiles to assist with donor development, stewardship, and direct communications and fundraising strategy. Uses a database or Customer Relationship Management (CRM) system to maintain research data and donor records, execute mailing or e-mail campaigns, and create reports. Additionally, Donor Research Coordinator maintains confidentiality and complies with data privacy regulations and policies. Requires a bachelor's degree. Typically reports to a manager. The Donor Research Coordinator occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. To be a Donor Research Coordinator typically requires 2-4 years of related experience. (Copyright 2024 Salary.com)

Recently Added Donor Research Coordinator jobs

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Clinical Research Coordinator III
  • DM Clinical Research
  • Jersey, NJ FULL_TIME
  • Clinical Research Coordinator III

    A CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.


    DUTIES & RESPONSIBILITIES
    • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
    • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
    • Sponsor-provided and IRB-approved Protocol Training
    • All relevant Protocol Amendments Training
    • Any study-specific Manuals Training, as applicable
    • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
    • Conducting and overseeing study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
    • Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
    • Completing and overseeing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
    • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
    • Demonstrated understanding, implementation and supervision of protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory for assigned protocols.
    • Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives for assigned protocols.
    • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
    • Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
    • Ability to train and mentor site staff, as needed
    • Supervise visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
    • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
    • Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
    • Maintaining a working knowledge of Study Participants’ Scheduling, Visit Tracking, Stipends and Transportation by liaising with the Administrative team.
    • Maintaining a working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
    • Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
    • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
    • Being prepared for and available at all required company meetings.
    • Submitting required administrative paperwork per company timelines.
    • Occasionally attending out-of-town Investigator Meetings
    • Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
    • Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
    • Facilitate effective communication between patients, healthcare providers, and research staff
    • Any other matters as assigned by management

    KNOWLEDGE & EXPERIENCE

    Education:
    • High School Diploma or equivalent required
    • Bachelor's degree preferred
    • Foreign Medical Graduates preferred
    Experience:
    • Minimum of 5 years experience in Clinical Research
    • Supervisory experience preferred
    • Wide therapeutic range of clinical trials experience preferred
    • Regulatory research experience is a plus
    Credentials:
    • ACRP or equivalent certification is preferred
    Knowledge and Skills:
    • Goals-driven while continuously maintaining quality.
    • Must be detailed-oriented, proactive, and able to take initiative.
    • Must have strong written and communication skills.
    • Must have excellent customer service skills.
    • Proficient communication and comprehension skills both verbal and written in the English language are required.
    • Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.
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Clinical Research Coordinator I
  • DM Clinical Research
  • Jersey, NJ FULL_TIME
  • Lab TechnicianThe Lab Technician will be responsible for assisting the clinical research staff in conducting clinical research trials.Duties & Responsibilities:Prepares, processes, and ships laborator...
  • 4 Days Ago
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Donor Relations Coordinator
  • New Jersey Institute of Technology
  • Newark, NJ FULL_TIME
  • Title:Donor Relations CoordinatorDepartment:VP Development & Alumni RelationsReports To:Director, Donor RelationsPosition Type:StaffPosition Summary:Provides administrative support to both the Directo...
  • 1 Month Ago
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Research Coordinator
  • FirstService Residential
  • Eatontown, NJ FULL_TIME
  • Job Overview: As a Marketing Research Coordinator, you'll be responsible for working via online and telephone resources to generate sales lead information based on identified opportunities within the ...
  • 1 Month Ago
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Nurse Care Coordinator, Living Donor Institute
  • RWJBarnabas Health
  • Brunswick, NJ PER_DIEM
  • RWJBH is seeking a Nurse Care Coordinator in the Living Donor Institute at the New Brunswick campus. This is a per diem, day shift position.Job Responsibilities:The Independent Living Donor Advocate I...
  • 26 Days Ago
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Billing Coordinator (Princeton, NJ - Remote/Hybrid Eligible)
  • Mathematica Policy Research
  • Princeton, NJ FULL_TIME
  • Position Description: Mathematica currently has an opening for a Billing Coordinator! We are searching for a Billing Coordinator to assist in the completion of all facets of the billing and collection...
  • 9 Days Ago
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Donor Research Coordinator jobs at Popular Companies

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Research Coordinator
  • NYU Langone Health
  • New York, NY
  • NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of...
  • 4/23/2024 12:00:00 AM
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Research Coordinator - Research Operations
  • Denver Health
  • Denver, CO
  • We are recruiting for a Research Coordinator - Research Operations to join our team! We are here for life's journey. Whe...
  • 4/22/2024 12:00:00 AM
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Research Coordinator (Research Professional 3)
  • University of Minnesota
  • Minneapolis, MN
  • About the Job Job Duties/Responsibilities: * Screen and recruit clinical trial subjects by pre-screening clinic patients...
  • 4/22/2024 12:00:00 AM
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Clinical Research Coordinator/ Research Nurse
  • M3 Global Research
  • Durham, NC
  • Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meetin...
  • 4/22/2024 12:00:00 AM
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Clinical Research Coordinator (Research Professional 1)
  • University of Minnesota
  • Minneapolis, MN
  • About the Job The primary purpose of the Clinical Research Coordinator (Research Professional 1) position includes: cond...
  • 4/22/2024 12:00:00 AM
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Community Outreach Research Coordinator/Research Associate - Administrative
  • Compu-Vision Consulting, Inc.
  • Santa Monica, CA
  • Title: Community Outreach Research Coordinator Location: 1399 S Roxbury Drive, Suite 100, Los Angeles, CA 90035 Duration...
  • 4/20/2024 12:00:00 AM
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Research Coordinator
  • NYU Langone Health
  • New York, NY
  • NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of...
  • 4/20/2024 12:00:00 AM
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Research Coordinator
  • Leidos
  • San Diego, CA
  • Description Are you looking for a career that will make an impact? The Leidos Military and Veterans Health Solutions Ope...
  • 4/9/2024 12:00:00 AM
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About New Jersey

New Jersey is bordered on the north and northeast by New York (parts of which are across the Hudson River, Upper New York Bay, the Kill Van Kull, Newark Bay, and the Arthur Kill); on the east by the Atlantic Ocean; on the southwest by Delaware across Delaware Bay; and on the west by Pennsylvania across the Delaware River. New Jersey is often broadly divided into three geographic regions: North Jersey, Central Jersey, and South Jersey. Some New Jersey residents do not consider Central Jersey a region in its own right, but others believe it is a separate geographic and cultural area from the Nor...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Donor Research Coordinator jobs
$63,358 to $82,137

Most Popular Cities in New Jersey for Donor Research Coordinator Jobs