Research Paramedic, Emergency Medicine, High Point Position Available In [Unknown county], North Carolina
Tallo's Job Summary:
Job Description
We’re excited to announce an internal opportunity for a full-time Research Paramedic to join our High Point ED site, supporting a dynamic portfolio of emergency and acute care trials. We offer flexible scheduling options – choose from five 8-hour shifts or four 10-hour shifts, with an end time of 9 PM or later to support evening coverage. As a Research Paramedic, you’ll play a vital role in the success of diverse studies across areas such as cardiac, trauma, neurology, and biomarker research.
Your day-to-day responsibilities could include:
Patient screening and identification Informed consent and enrollment Performing protocol procedures Specimen collection and lab processing Documentation, data entry, and study compliance Collaboration with ED teams, research staff, and investigators
JOB SUMMARY
Under departmental direction, coordinates activities to support multiple research studies of all phases. Serves as the principal administrative liaison for assigned studies with the ability to manage a workload that includes studies of increased complexity. Perform study procedures in accordance with NCCEP protocols set forth by the N.C. Office of EMS (NCOEMS). Develops and maintains recordkeeping systems and procedures to ensure compliance with study protocols and all appropriate regulations. Attends clinic as needed to perform activities including, but not limited to: assist the research team with recruitment activities, administer questionnaires or medications, perform blood draws and answer any questions about future appointments. Responsible for the compilation, registration and submission of data, as required by the Sponsor.
EDUCATION/EXPERIENCE
Paramedic certification from an accredited certified paramedic program, or an Associate’s degree of Applied Science (A.A.S.) in paramedic studies or equivalent. Three years of Emergency Service experience preferred. Bachelor’s degree preferred LICENSURE, CERTIFICATION, and/or
REGISTRATION
Basic Cardiac Life Support (BCLS) and NC-OEMS certification as EMT-P required. Advanced Cardiac Life Support (ACLS) or Pediatric Advanced Life Support (PALS) may be required within one year in select areas. Critical care certificate or national registry paramedic, preferred. Maintains certification through affiliation with approved NC-OEMS education provider.
ESSENTIAL FUNCTIONS
Works under the direction of the Study Investigators or Clinical Research Nurse Manager with minimal supervision. Uses medications, treatments and protocols within the scope of practice as defined by NCOEMS, under the orders from a physician. Documents any medication and treatment rendered in the Electronic Medical Record. Abstracts data from the medical record and completes paper and electronic case report forms, including responding to any requests for data clarification, and maintains all necessary source documents. Follows established Wake Forest Baptist and department policies, procedures, objectives, performance improvement, attendance, safety, environmental, and infection control guidelines, including adherence to the workplace Code of Conduct and Compliance Plan. Practices a high level of integrity and honesty in maintaining confidentiality. Plays an active role in recruitment of patients to study. Performs protocol specific duties required per the research protocol Fulfills sponsor requirements related to reportable information including adverse events, unanticipated problems, and other information required by the sponsor protocol. Obtains or assists the Principal Investigator in obtaining informed consent from subjects and reinforces the information that has been provided to subjects and families. Provides staff relief as required to meet the needs of the department. Participates in scheduled team/department meetings. Participates in quality improvement projects on an on-going basis Identifies and communicates important protocol and data management issues or problems to the supervisor in a timely manner. Performs other related duties as assigned or requested.
SKILLS & QUALIFICATIONS
Excellent interpersonal, oral, and written communication skills Excellent reading comprehension Strong organizational skills EPIC/WakeOne proficiency to include appropriate documentation of research notes Proficient in the use of OnCore/WISER Clinical Trial Management System Basic computer skills Fosters/promotes a positive image and professional appearance Sensitivity to intercultural relations Sensitivity to the maintenance of confidentiality Knowledge of Microsoft Products
WORK ENVIRONMENT
Combination of academic office and exam/procedure room settings Well-lighted, well-ventilated, and adequate space Frequent exposure to diseases, medicinal preparations and other conditions common to a clinic environment