Job Overview
Responsibilities:
- Coordinate enrollment and obtain signed consent forms from patients or research participants recruited to assigned research project(s).
- Provide organized support to the research team.
- Attend all assigned training meetings; may involve travel.
- Assist in identifying strategies and tactics to implement assigned research project with an emphasis on accuracy and safety.
- Carry out experimental or clinical interventions, clinical assessment and data collection procedures with research participants.
- Identify educational needs of research participants and other research team members
- Provide training to research team with materials/tools available from project principal investigators.
- Maintain appropriate documentation and study records.
- Comply with data collection and record keeping standards outlined in IRB-approved protocols.
- Maintain privacy, confidentiality, accuracy, objectivity, and professionalism in all written documentation and medical records
- Documents and communicates Adverse Events (AEs) and Serious Adverse Events (SAEs) and unanticipated problems in a timely manner in accordance with regulatory and protocol requirements. Communicate with all parties in a timely and accurate manner to the Study Coordinator, Investigator, IRB or other appropriate members of the research team to ensure the health, safety and welfare of the participant(s).
- Licensed healthcare professional (State of Florida) PT as required for specific designated projects.
- Basic Life Support (BLS) certification required.
- At least one year of recent clinical experience.
- Discipline-specific clinical skills and experience required
- Requires self-motivation and initiative skills, excellent verbal/written communication, desktop computing and operation skills.
- Human subject research related experience preferred.
Company Info
