Memorial Medical Center
Plans, develops, and oversees the day-to-day clinical activities for a specified clinical trials initiative and/or other medical research program in accordance with the research parameters established by the investigator. Develops and administers operating procedures for the project, coordinates project funding and day-to-day interactions with associated departments and agencies, and oversees patient recruitment, education, and administration. Coordinates implementation and execution of study protocol, and oversees all aspects of the provision of patient care to participants, in compliance with protocol requirements. Oversees and supervises clinical research team (includes Research RNs and Data Coordinator).
Oversees the planning, scheduling, and carrying out of day-to-day clinical activities and procedures, ensuring workflow and adequate care and treatment of research subjects.
Ensures that all clinical activities are carried out in accordance with established research protocol and standards and in compliance with applicable laws, regulations, policies, and procedural requirements.
Oversees and provides direct nursing evaluation and/or other related care and consultation to patients as required.
Administers prescribed study medications, monitors vital signs, and/or performs other specialized nursing procedure, as appropriate to the specific needs of the study and individual subjects.
Monitors and records patient response to treatment, and communicates study data and results to investigators; maintains source documentation and oversees the preparation of study activity reports for sponsors and various medical, legal and regulatory bodies, as appropriate.
Oversees and coordinates the recruitment, care, and treatment of patient research subjects; coordinates services with other internal departments and allied service agencies.
Supervises personnel, which typical includes recommendations for hiring, firing, performance evaluation, training, work allocation, and problem resolution.
Establishes appropriate data collection systems and procedures, according to pre-established research protocol; coordinates and monitors the collection, processing, and recording of clinical data and/or specimen samples, as required by established study protocol.
Coordinates, plans, and implements clinical pharmaceutical protocol for the study; monitors study activity and prepares reports to funding agencies and investigators as appropriate.
Assesses operational, financial, and material requirements for studies and develops budges and funding mechanisms as appropriate.
Serves as primary joint of liaison and coordination between investigators, ancillary departments, research subjects, sponsoring organizations, and/or regulating bodies.
Performs miscellaneous job-related duties as assigned. LifePoint Health is committed to providing Equal Employment Opportunities for all applicants and employees and complies with all applicable laws prohibiting discrimination against any employee or applicant for employment because of color, race, sex, age, religion, national origin, disability, genetic information, gender identity, sexual orientation, veterans’ status or any other basis protected by applicable federal, state or local law.