We use cookies. Find out more about it here. By continuing to browse this site you are agreeing to our use of cookies.
Back to search results

Patient Coordinator

Cape Fox Shared Services
United States, Maryland, Rockville
Apr 04, 2025

Concentric Methods is seeking a Patient Coordinator to join our team in Bethesda, MD in support of the NIH.

Responsibilities:



  • Coordinates the recruitment, scheduling, travel and admission of research study participants.
  • Work with staff to coordinate new research patient screening appointments, procedures and imaging studies between protocol investigators and the outpatient clinic scheduling personnel.
  • Coordinate scheduling, travel and lodging of subjects participating in studies. 2
  • Track patient referral process by maintaining patient/volunteer spreadsheets.
  • Schedule diagnostic Appointments.
  • Coordinate volunteer payments.
  • Coordinate patient schedules with testers, nurses, physicians and clinical research coordinators.
  • Act as primary point of contact for patients enrolled in the study.
  • Coordinate the recruitment, scheduling, travel and admission of research study participants with clinical staff.
  • Distributes recruitment materials.
  • Distribute patient recruitment and communication materials.
  • Acts as a liaison between participants, participant's relatives and staff members and communicates participant's questions, complaints, problems and concerns to appropriate staff members.
  • Triage questions to appropriate personnel in the team as necessary.
  • Maintain ongoing relationships with patients, families, caregivers, medical care providers and various individuals on a continuous long-term basis.
  • Respond to patient emails and phone calls; prioritize patient related issues into urgent, emergent and routine; triage the issues to the appropriate personnel in the team as necessary.
  • Assist with navigating patients to their appointments.
  • Coordinate NIH resources designated for Epilepsy Service use and communication of requirements to different staff groups and departments.
  • Troubleshoot scheduling issues to ensure maximum productivity of staff resources.
  • Understand protocol requirement changes, and schedule participants for new/updated appointment and procedures accordingly.
  • Prepare, maintain, and fax weekly schedule; ensure that all protocol specifics are completed.
  • Explains policies and procedures to participants and refers them to appropriate staff.
  • Serve as point of contact for questions, advice and communications on the process and status of protocols; initiate and respond to correspondence and telephone contacts pertaining to admission of patients.
  • Explain the purpose of the study to potential participants; assess eligibility to participate; enroll eligible study participants and explain the research procedures; respond to routine questions on study procedures and seek additional information when needed.
  • Respond to communications with research subjects; direct questions to appropriate team member.
  • Understand protocol requirement changes, and explain rationale to participants when scheduling new/updated appointment and procedures.
  • Collates, enters and maintains data collected on participants.
  • Collect, verify, record and maintain data on clinical activity and/or research.
  • Collect outside medical documentation, electronically scans and uploads records into the electronic medical record.
  • Collate and enter data collected on participants.
  • Ensure accurate and complete collection and submission of study data
  • Maintain patient files, medical records, and patient family contacts; file medical record notes into patient charts daily.
  • Maintain clinical data in protocol databases.
  • Create reports/spreadsheets for tracking and scheduling of protocol patients.
  • Review patient and clinical charts; enter patient data into files and automated databases.
  • Ensure that research data are entered into database.
  • Ensure consistency in records, data and datasets in accordance with regulatory requirements.
  • Work with staff on QA/QC of the clinical and research records for patients on study prior to audits.
  • Obtain medical information, imaging disks and pictures from applicants on an ongoing basis; file them with the records.
  • Track patient referral process by maintaining patient/volunteer spreadsheets.
  • Maintain protocol files (electronic and hard copies).
  • Assist with sending and receiving patient records.
  • May assist with gathering documents for IRB/FDA review.
  • Coordinates new patient referrals by obtaining pertinent information and forwarding it for review.
  • Provide lists of potential research volunteers to principal investigators based on database searches against protocol criteria.
  • Refer prospective volunteers per study guidelines to the appropriate Institute contact person.
  • Review incoming patient referrals and contact referring physician's office if referral is incomplete.
  • Obtain outside medical records, radiology studies, biopsy slides and submit to the respective departments at the NIH.
  • Communicate with appropriate staff about intake and materials and submission of materials for review.
  • Screen calls from patients, physicians, and callers from the public; forward to appropriate staff members; update patient telephone directory as needed.
  • May assist in preparing credentialing packages.
  • May assist Office Manager and Administrative Officer with documentation for credentialing packages.
  • Monitors workflow and administers and revises processes to maintain and improve operations.
  • Work with staff to achieve optimum schedule and staff utilization; work with staff in problem solving for overlapping appointments.
  • Review future scheduled cases to resolve potential conflicts or problems; monitor additional reports to ensure data validity.
  • Troubleshoot scheduling issues to ensure maximum productivity of staff resources.
  • Monitor and identify areas of improvement in the clinic environment, clinical trial conductance in the outpatient setting, for patients, families and staff.
  • Participate in training other clinical staff on clinical operations.
  • Participate in quality improvement initiatives and maintenance of SOPs.
  • Mentors and trains staff on patient recruitment and coordination processes and procedures.
  • Assesses organizational need and develops or updates detailed manual of procedure (MOP) or standard operating procedure (SOP) on patient recruitment and coordination processes and procedures.
  • Arrange patient scheduling, travel and admissions as designated by each specific protocol
  • Track patient referral process by maintaining patient volunteer spreadsheets
  • Screen calls from patients, physicians and callers from the public; forward to appropriate staff members; update patient telephone directory as needed
  • Schedule diagnostic appointments
  • Enter patient data into database
  • Maintain clinical data in protocol databases
  • Maintain patient files
  • Coordinate volunteer payments
  • Prepare, maintain and fax weekly schedule; ensure that all protocol specifics arecompleted
  • Prepare documents for clinical protocols in IRBFDA
  • Maintain protocol files electronic and hard copies
  • Assist with training of new staff
  • Execute protocol changes in patient population
  • Create reports spreadsheets for tracking and scheduling of protocol patients
  • Coordinate NIH resources designated for Epilepsy Service use and communication of requirements to different staff groups and departments
  • Troubleshoot scheduling issues to ensure maximum productivity of staff resources


Applied = 0
#alert

(web-77f7f6d758-swlff)