Donor Research Coordinator, Sr. jobs in Kingsport, TN

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)

H
Clinical Research Coordinator
  • HMG
  • Kingsport, TN FULL_TIME
  • General Summary:
    The Clinical Research Coordinator is responsible for managing clinical research activities. They will screen and enroll subjects ensuring they meet inclusion and exclusion criteria. Manage study related activities, ensure subject compliance and prepare documentation. The Clinical Research Coordinator will also monitor and report adverse events to the appropriate staff members as well as complete end of study regulatory documentation.

    Main Responsibilities:
    Under the direction of the Principal or Sub-investigator, manage the conduct of clinical research activities.
    Develop management systems and prepare for study initiation
    • Assess study feasibility in terms of study's impact on site resources, labor cost, cost by procedure, potential for problems (such as serious AEs, noncompliance, willingness of subjects to participate, protocol deviations, etc.)
    • Possess a comprehensive and in-depth understanding of each protocol that has been assigned as a primary responsibility;
    • Review with the principal investigator the inclusion/exclusion criteria, overall structure, and requirements of each protocol;
    • Review the protocol summary sheet and the informed consent form for accuracy and clarity;
    • Develop source documents based on the most current IRB approved protocol and reviewed for accuracy and clarity;
    • Develop a plan for subject recruitment and ongoing communications with primary care physicians and nursing staff, as appropriate.
    Screen and enroll study subjects
    • Review the study design and inclusion/exclusion criteria with the subject’s primary physician;
    • Review and verify all relevant source documentation in the subject's medical record to confirm study eligibility;
    • Review the protocol, informed consent form, and follow-up procedures with potential study subjects;
    • Ensure the current approved informed consent is signed before subjects are screened and enrolled;
    • Ensure that the randomization procedure is followed as per protocol guidelines;
    • Document protocol exemptions and deviations and report to IRB (as required).
    Manage study related activities, subject compliance and documentation
    • Including related clinical duties such as performing EKGs, lab processing, and if not already qualified to perform phlebotomy – must acquire these skills.
    • Ensure adherence to protocol requirements;
    • Schedule subjects for follow-up visits;
    • Assist investigators in assessment of subject response to therapy;
    • Review laboratory data, inform investigator of abnormal values and document;
    • Report to primary care provider as appropriate;
    • Assess and document subject compliance with medications and visits;
    • Communicate with pharmacy staff to assure timely and accurate study drug distribution;
    • Manage administration of investigational therapy;
    • Maintain dispensing logs (if allowed);
    • Maintain copies any documentation for dispensing of investigational products and/or study-related supplies;
    • Oversee specimen collection, storage, and shipment;
    • Attend study-related meetings as appropriate;
    • Communicate regularly with the principal investigator, monitor (others responsible for conduct of the research) about study-related issues.
    Record data and study documentation
    • Record data as directed using the appropriate media or platform;
    • Follow procedures for access and security for electronic data entry;
    • Review keyed data for accuracy as needed;
    • Send data to the data collection center on a timely basis;
    • Maintain source documentation for all data entered, including clinic chart visit notes, lab data, and procedure reports;
    • Correct and edit data as directed and as appropriate.
    Monitor and report adverse events
    • Document and record all AEs as outlined in protocol with causality determined by PI or SI.
    • Report serious adverse events (SAEs) to the principal investigator, sponsor, and IRB (others as required by funding source or as outlined in the protocol).
    Regulatory documentation
    • Know and understand all regulatory requirements associated with the conduct of the study assigned;
    • Maintain files and documents as regulations dictate;
    • Prepare and submit initial applications to central and local committees (IRBs, biosafety, radiology, etc), prepare and submit reports as required;
    • Ensure that all required documentation is complete and appropriately filed.
    Management of site activities during audits and inspections
    • Prepare for quality assurance audits and regulatory inspections as needed;
    • Act as contact person before, during, and after audits and inspections;
    • Provide all required documentation to auditors;
    • Make all appropriate corrections as requested by auditors;
    • Coordinate site response to audit / inspection findings.
    Management of ancillary staff
    • Train and supervise support staff (e.g., research assistants, clerical staff and volunteers).

    Education/Experience/Knowledge:
    • 2 year Degree or appropriate experience related to anticipated duties
    • Experience in the conduct of clinical research preferred but not required for application.
    • Interpersonal and communication skills - interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources.

    Physical/Mental Demands:

    To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

     

    Essential: Communication with others to exchange or express information and ideas. Ability to receive detailed information through oral communication, and to make fine distinctions in sounds. Determine the accuracy, neatness, thoroughness of the work assigned and perceive general observations. Remaining upright on the feet, particularly 75% of the time. Moving about on foot to accomplish tasks. Bending body downward and forward by bending spine at the waist and/ or by bending leg and spine. Extending the hands and arms in any direction. Exerting force upon an object so that an object moves away/toward the force. Picking, pinching, typing or otherwise working, primarily with fingers. Applying pressure to an object with the fingers and palm. Perform a variety of duties, often changing from one task to another of a different nature. Perform with frequent interruptions and/ or distractions. Make appropriate job decisions following standard office policies and past precedents. Adjust priorities quickly as circumstances dictate. Ability to establish and maintain cooperative working relationships with co-workers and the public. Ability to interact appropriately with colleagues and patients for different purposes and different context.

     

    Marginal: Must be able to remain in a stationary position at least 25% of the time. Medium work that includes moving objects up to 50 pounds occasionally. Perceiving attributes of objects, such as size, shape, temperature, or texture by touching with skin, particularly that of fingertips. Work independently and identify potentially more effective methods of work operations. Observing an area that can be seen up and down or to right or left while eyes are fixed on a given point. Ability to identify and distinguish colors.

    Disclaimer:

    The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification.  They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Management reserves the right to revise the job or to require that other or different tasks be performed as assigned.

    All job requirements are subject to possible revision to reflect changes in the position requirements or to reasonably accommodate individuals with disabilities.

  • 2 Months Ago

B
Manager, Donor Center
  • BioIVT
  • Gray, TN FULL_TIME
  • SUMMARY This position will assist with the development and implementation of policies and procedures relating to donor center operations. Provides direction, training and mentoring to team to facilita...
  • 18 Days Ago

K
Coordinator
  • K-VA-T Food Stores Inc
  • Johnson, TN FULL_TIME
  • Essential Job Functions : Ensure efficient and courteous customer service at all times in support of the company mission to Run the Best Store in Town! Maintain a positive attitude; create an atmosphe...
  • Just Posted

K
Coordinator
  • K-VA-T Food Stores Inc
  • Blountville, TN FULL_TIME
  • Essential Job Functions : Ensure efficient and courteous customer service at all times in support of the company mission to Run the Best Store in Town! Maintain a positive attitude; create an atmosphe...
  • 3 Days Ago

P
Sr. Construction Manager
  • Parsons Government Services Inc.
  • Kingsport, TN FULL_TIME
  • In a world of possibilities, pursue one with endless opportunities. Imagine Next! When it comes to what you want in your career, if you can imagine it, you can do it at Parsons. Imagine a career worki...
  • 19 Days Ago

F
Sr. Project Engineer
  • Food Management Search
  • Johnson, TN FULL_TIME
  • Currently, we are looking for an Sr. Project Engineer based in Johnson City, Tennessee.Our client, founded in 1874, is a $3.5 billion publicly traded technology leader with over 12,000 employees globa...
  • 9 Days Ago

Filters

Clear All

  • Filter Jobs by companies
  • More

0 Donor Research Coordinator, Sr. jobs found in Kingsport, TN area

R
Clinical Research Coordinator (FT) Days, Research & Academics - Kingsport, TN
  • Research and Academics
  • Kingsport, TN
  • Clinical Research Coordinator (FT) Days, Research & Academics - Kingsport, TN Job ID: 004EKT BALLAD CORPORATE Nursing - ...
  • 3/28/2024 12:00:00 AM

F
LPN/CMA/RMA-Physician Practice (FT) Colonial Heights, TN
  • First Assist Colonial Heights
  • Kingsport, TN
  • LPN/CMA/RMA-Physician Practice (FT) Colonial Heights, TN Job ID: 004E73 BLUE RIDGE MEDICAL MANAGEMENT Nursing - First As...
  • 3/28/2024 12:00:00 AM

F
CNA/Nursing Assistant (FT) 3p-11p Family Birth - Johnson City, TN
  • Family Birth Center
  • Johnson City, TN
  • CNA/Nursing Assistant (FT) 3p-11p Family Birth - Johnson City, TN Job ID: 004AN7 FRANKLIN WOODS COMMUNITY HOSPITAL Nursi...
  • 3/28/2024 12:00:00 AM

W
LPN/CMA/RMA-Physician Practice (FT) WCS Outpatient Clinic - Johnson City, TN
  • WCS Outpatient Clinic Johnson City SOF
  • Johnson City, TN
  • LPN/CMA/RMA-Physician Practice (FT) WCS Outpatient Clinic - Johnson City, TN Job ID: 004EBS CARDIOVASCULAR ASSOCIATES Nu...
  • 3/28/2024 12:00:00 AM

B
Pharmacist, Clinical Spec. *SIGN ON BONUS PGY-2* (FT) Pediatric-Johnson City, TN
  • Ballad Health
  • Johnson City, TN
  • Pharmacist, Clinical Spec. *SIGN ON BONUS PGY-2* (FT) Pediatric-Johnson City, TN Job ID: 004DN4 NISWONGER CHILDRENS HOSP...
  • 3/28/2024 12:00:00 AM

W
LPN/CMA/RMA-Physician Practice (FT) WCS CVT Surgery - Johnson City, TN
  • WCS CVT Surgery Johnson City
  • Johnson City, TN
  • LPN/CMA/RMA-Physician Practice (FT) WCS CVT Surgery - Johnson City, TN Job ID: 004ECY CARDIOVASCULAR ASSOCIATES Nursing ...
  • 3/28/2024 12:00:00 AM

B
LPN/CMA/RMA-Physician Practice (PRN) Float
  • BHMA Float Pool
  • Johnson City, TN
  • LPN/CMA/RMA-Physician Practice (PRN) Float Job ID: 004DXG BLUE RIDGE MEDICAL MANAGEMENT Nursing - BHMA Float Pool PRN, A...
  • 3/28/2024 12:00:00 AM

B
LPN - Physician Practice (FT) BHMA Float Pool - Johnson City, TN
  • BHMA FLOAT POOL
  • Johnson City, TN
  • LPN - Physician Practice (FT) BHMA Float Pool - Johnson City, TN Job ID: 00432T BLUE RIDGE MEDICAL MANAGEMENT Nursing - ...
  • 3/28/2024 12:00:00 AM

Kingsport is located in western Sullivan County at 36°32′N 82°33′W / 36.533°N 82.550°W / 36.533; -82.550 (36.5369, −82.5421), at the intersection of U.S. Routes 11W and 23. Kingsport is the northwest terminus of Interstate 26. US 11W leads east 22 miles (35 km) to Bristol and southwest 28 miles (45 km) to Rogersville, while US 23 leads north 38 miles (61 km) to Big Stone Gap, Virginia. I-26 and US 23 lead south 8 miles (13 km) to Interstate 81 and 83 miles (134 km) to Asheville, North Carolina. The city is bordered to the west by the town of Mount Carmel, to the southeast by unincorporated ...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Donor Research Coordinator, Sr. jobs
$67,185 to $90,384
Kingsport, Tennessee area prices
were up 1.3% from a year ago

Donor Research Coordinator, Sr. in Alamogordo, NM
This will entail close examination of incoming gifts, ongoing communication with gift officers regarding donor intent and interests, and frequent interaction with the offices of the Managing Director.
December 15, 2019
Donor Research Coordinator, Sr. in Monroe, LA
Garnering the attention of influential people who are personally affected by diabetes, the Foundation has grown into an international coalition of business leaders, celebrities, scientists, clinicians, families and other concerned individuals who have elevated the importance of cure-focused research and provided meaningful support for the DRI's multidisciplinary research program.
February 06, 2020
Donor Research Coordinator, Sr. in Sacramento, CA
The Diabetes Research Institute Foundation was created for one reason - to cure diabetes - which is and will continue to be its singular focus until that goal is reached.
January 03, 2020