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Clinical Research Coordinator

Dayton Physicians Network
Kettering, OH Full Time
POSTED ON 4/16/2026
AVAILABLE BEFORE 5/15/2026
Dayton Physicians Network is looking to add a Clinical Research Coordinator to our team!

Schedule: Monday through Friday 8:00am - 4:30pm

No weekends, evenings or holidays!

Work/life balance schedules

Why work for Dayton Physician's Network?

  • Full-time employees are eligible for health, dental and vision benefits
  • Company holidays and a flexible holiday!
  • Generous Paid Time Off (PTO) Package
    • Additional accrual increase after 1 year of service with Dayton Physicians!
  • 401K
  • Scrub Allotments
  • Yearly Bonus Program
  • Dayton Physicians Network as an Independent Practice <--- Watch video here!
  • DPN Core Value Expectations:

    The CARES model reflects the principles that guide our day-to-day behaviors; our decisions, our actions, and our relationships with each other and with the patients and families we serve. All DPN employees are expected to embrace and demonstrate the following:

    • COMPASSION: the patient is at the center of all we do
    • ACCOUNTABILITY: we hold ourselves accountable for our actions
    • RESPECT: we show respect for others
    • EXCELLENCE with Innovation: we strive for excellence in all we do
    • SERVICE through Collaboration: we provide service to our patients, team members and community.


    Essential Duties and Responsibilities:
  • Coordinates screening and enrollment of clinical trial patients.
    • Reviews physician patient schedules and assesses patients for possible clinical trial enrollment.
    • Educates patients and families during the informed consent process.
    • Registers patients and participants to protocols.
    • Ensures eligibility requirements are met and reviews with physician investigator.
    • Ensures protocol required patient testing is ordered and complete.
    • Maintains record of recruitment strategies.
    • Markets protocols as needed to meet recruitment goals.
  • Coordinates clinical trial activities
    • Gathers and verifies source documents
    • Verifies the accuracy, completeness and timely submission of case report forms.
    • Collaborates with investigator to ensure protocol compliance in patient selection, treatment, dose modifications and response.
    • Interviews patient to assess adverse events, medication compliance, and patient reported outcomes.
    • Obtains follow-up data required when patient is off active treatment.
    • Maintains investigational drug (IND) inventory
    • Reviews protocols and assesses current inventory of IND.
    • Maintains inventory on individual drug accountability records.
    • Ensures treatment order is correct by reviewing protocol guidelines and calculating dose prescribed.


  • Gathers, completes, and tracks investigator required forms that comply with federal, and institutional guidelines. Ensures physician investigators complete required protocol training prior to patient enrollment.
  • Coordinates credentialing of laboratory, radiology and radiation equipment as required by protocol.
  • Use research database to track patient enrollments, patient demographics and status. Run reports to provide to information to physician investigators and administrator.
  • Disseminates protocol information.
    • Reviews and educates physician investigators on new protocol activations, closures, and revisions.
    • Serves as a professional resource regarding clinical trials, protocol procedures and protocol compliance for investigators, nurses, pharmacists, pathologists, radiologists and other health care personnel.
  • Demonstrates clinical competency by providing direct patient care as required by protocol. (EKGs, vitals, lab draws). Obtains protocol specific training as required to enroll patients on clinical trials.
  • Order and track laboratory kits needed for research related blood draws. Process and ship specimens as required by protocol. Maintain hazardous materials education certification.
  • Travel between locations as needed.
  • Performs other duties as assigned.

Required Education and/ or Experience:

A bachelor’s degree in nursing or other health-related field is preferred. Pertinent LPN or RN licensure/registration must be maintained. Previous research experience and/or recent nursing experience is preferred.

General Skill Requirements:

  • Excellent oral and written communication
  • Working knowledge of Microsoft Office, including Word, Excel and Outlook.
  • Experience working with a Practice Management system.
  • Attendance and punctuality are essential requirements of this position to provide excellent customer service to both our internal and external stakeholders.

Salary.com Estimation for Clinical Research Coordinator in Kettering, OH
$57,399 to $75,253
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