Donor Research Coordinator, Sr. 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, Sr. 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, Sr. maintains confidentiality and complies with data privacy regulations and policies. Requires a bachelor's degree. Typically reports to a manager. The Donor Research Coordinator, Sr. work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Donor Research Coordinator, Sr. typically requires 4-7 years of related experience. (Copyright 2024 Salary.com)
Title :
Tissue Donor Coordinator
BELONG. CONNECT. GROW. with KBR.
Around here, we define the future. We are a company of innovators, thinkers, creators, explorers, volunteers, and dreamers.
But we all share one goal : to improve the world responsibly and safely.
KBR is seeking a Tissue Donor Coordinator to support our SPARC Program for KBR’s Science and Space division. The SPARC program (Service Personnel Advancing Research on CTE) seeks to : 1) Provide education to service members, veterans, and their families on brain donation;
2) Register individuals for participation in the Brain Donation Awareness Registry; and 3) Recover whole specimens, process, and prepare for shipping using appropriate methods.
The goal of this program is to support research that is ongoing at the Uniformed Services University’s Brain Tissue Repository related to military brain injury and chronic traumatic encephalopathy.
This position offers a hybrid work schedule.
Under the direction of the Senior Program Manager (SPM), Senior Neuroscientist, and contract project manager(s), the Tissue Donor Coordinator will supervise Donor Specialists, Tissue Recovery Technicians, Marketing Specialists, and Peer / Family Educators on site, ensure clear communication with leadership and peers, and maintain compliance with regulatory accreditation agencies and internal quality processes on site.
The Tissue Donor Coordinator will establish relationships with local coroners, justice of the peace, medical examiners, and tissue procurement organizations to develop protocols to support logistics surrounding tissue acquisition and processing with guidance from Neuroscientist.
The Tissue Donation Coordinator will ensure compliance with protocols and report progress back to the Neuroscientist.
This position will be on-call on a rotating and regular basis.
Supervisory Responsibilities :
General Administrative Responsibilities :
Maintains proof of all such education for all engaged members of the study team. Coordinates with staff to help ensure that clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures.
Assists in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan.
Maintains documentation of training.
Protocol and Review :
These study materials include but are not limited to the informed consent document, case report forms (CRFs), enrollment logs, and study data.
Establishes and organizes study files, including but not limited to, regulatory binders, case report forms, study specific source documentation.
Informed Consent :
Award Acceptance (Terms & Conditions) :
Reviews and develops a familiarity with the contract or award terms and conditions. Works to assure that the study is in compliance with all terms and conditions, including but not limited to education, IRB (HRPO) approval, conflict of interest disclosure, health and safety protections for participants and staff and any financial terms or conditions.
Conduct of Research :
Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.
Protected Health Information :
Assists PI to assure that all personnel complete appropriate training.
Cooperates with compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance to the appropriate compliance office.
Unanticipated Problems :
Assists in promptly reporting any unanticipated problems involving risks to research participants or others to the HRPO and IRB.
Reporting :
Project Closeout :
REQUIRED EDUCATION / EXPERIENCE :
Education : Must have a bachelor’s degree with at least 2 years of experience in human subject research or tissue donation.
An additional 8 years of experience will be accepted in lieu of a degree.
PREFERRED EDUCATION / EXPERIENCE :
Basic Compensation : $82,100-$123,200
$82,100-$123,200
The offered rate will be based on the selected candidate’s knowledge, skills, abilities and / or experience and in consideration of internal parity.
KBR is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, disability, sex, sexual orientation, gender identity or expression, age, national origin, veteran status, genetic information, union status and / or beliefs, or any other characteristic protected by federal, state, or local law.
Last updated : 2024-05-05