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Donor Research Coordinator jobs in Illinois

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
  • Chicago, IL 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.
  • 1 Day Ago
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Clinical Research Coordinator
  • Revival Research Institute, LLC
  • ELGIN, IL FULL_TIME
  • Unique opportunity to make an Impact in the healthcare industry… Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since...
  • 2 Months Ago
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Philanthropy Coordinator, Donor Relations
  • Northwestern Memorial Healthcare
  • Chicago, IL FULL_TIME
  • Company DescriptionAt Northwestern Medicine, every patient interaction makes a difference in cultivating a positive workplace. This patient-first approach is what sets us apart as a leader in the heal...
  • Just Posted
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Philanthropy Coordinator, Donor Relations
  • Northwestern Memorial Foundation
  • Chicago, IL FULL_TIME
  • DescriptionThe Philanthropy Coordinator reflects the mission, vision, and values of NM, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant po...
  • Just Posted
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Donor Care Coordinator
  • Hesed House
  • Aurora, IL FULL_TIME
  • Job Title: Donor Care Coordinator Ministry: Development Reports to: Division Director of Development FLSA Status: Salary Exempt Posted Date: June 23, 2023 ORGANIZATIONAL BACKGROUND At Hesed House, sav...
  • 1 Day Ago
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Donor Family Services Coordinator
  • Gift of Hope
  • Itasca, IL FULL_TIME
  • Overview Gift of Hope is proud to serve as the federally designated not-for-profit organ procurement organization (OPO) that coordinates organ and tissue donation and provides compassionate service to...
  • 1 Month Ago
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Donor Research Coordinator jobs at Popular Companies

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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...
  • 4/25/2024 12:00:00 AM
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Research Coordinator Supervisor
  • University of Southern California
  • San Diego, CA
  • Research Coordinator Supervisor Job Announcement This position is located in San Diego, CA. The Neuroscience Translation...
  • 4/24/2024 12:00:00 AM
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Clinical Research Coordinator
  • CARLE
  • Urbana, IL
  • The hEDS GENE Study is looking for a data analyst to assist in its ongoing efforts to identify genes associated with the...
  • 4/24/2024 12:00:00 AM
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Clinical Research Coordinator (Researcher 1)
  • University of Minnesota
  • Minneapolis, MN
  • About the Job Dr. Sabine Schmid in the Department of Psychiatry and Behavioral Sciences is seeking a part-time (4-6 hour...
  • 4/23/2024 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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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 Illinois

Illinois (/ˌɪlɪˈnɔɪ/ (listen) IL-ih-NOY) is a state in the Midwestern and Great Lakes region of the United States. It has the fifth largest gross domestic product (GDP), the sixth largest population, and the 25th largest land area of all U.S. states. Illinois is often noted as a microcosm of the entire United States. With Chicago in northeastern Illinois, small industrial cities and immense agricultural productivity in the north and center of the state, and natural resources such as coal, timber, and petroleum in the south, Illinois has a diverse economic base, and is a major transportation hu...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Donor Research Coordinator jobs
$59,138 to $76,666

Most Popular Cities in Illinois for Donor Research Coordinator Jobs