Frederick Moore Email & Phone Number

United States

• Lead and coordinate all aspects of the projects and future funded research. ALCOA++• Initiate and maintain all IRB protocols and activities.• Provide excellent customer service to patients and participants, healthcare partners, Investigators, sponsors, and vendors. • Supervision of clinical and non-clinical staff implementing studies. Staff supervision includes but is not limited to interviews/hiring new staff, management of staff and daily staff deliverables.• Assists clinical research coordinators and other research staff members in the timely and accurate completion of data and reports.• Coordinate and lead disease/topic specific research meetings and provide updates on clinical trial affairs with clinical research staff including principal investigators, co-investigators, managers, and coordinators.• Responsible for overseeing and managing data collection, analysis, and cleaning, performing regular audits to ensure that the data collected is complete and accurate, and that the research is being conducted as outlined in the protocol.• Mentor and supervise study coordinators, student researchers, and volunteers.• Perform: IP accountability and dosing, Venipuncture, Vitals, Injections, ECG, Spirometry, etc. as outlined per protocol.

Orlando, Florida, United States

• Hire, orient, train, and conduct performance reviews for staff handling research administration activities associated with the conducting of clinical trials. Monitor staffing levels and identify adequate coverage for trial workload across teams of study coordinators.• Supervise the implementation of and adherence to study protocols. Educate research staff on established policies, processes, and procedures.• Engage in outreach and networking opportunities, representing the research program to a variety of internal and external audiences.• Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes.• Covid-19 PCR testing, Phlebotomy, IV access, Vitals, Lab sample collection and processing, Medication administration. • Conducted training sessions for Research staff to refresh or hone needed skills to be better equipped to handle daily functions of assigned role: ECGs, vitals, venipuncture, and documentation, etc.

Orlando, Florida, United States

• Infectious disease treatment and prevention: HIV, Hep C, Syphilis, etc. Patient education on STDs/STIs. • Venipuncture, ECG, Intravenous access, vital signs, Triage, patient medication ordering, STD screening and treatment, Covid-19 PCR testing.• Assessing and identifying patients’ needs for prompt treatment for STDs/STIs.• Directed office flow to facilitate smooth patient experience. • Conducted office supply and medication order. • New Hire training and mentoring.

Daytona Beach, Florida, United States

* Initiate outreach outside of the phone system through email, text message, and future channels in an effort to engage potential patients to call us to initiate our screening process.* Utilize approved scripting and possess the ability to display soft skills to encourage potential patients to speak with a Nurse Coordinator.* Ensuring all patient enrollment activities are performed as per clinical trial protocol parameters by engaging directly with the CRCs and working closely with the clinical trial team.* Interfacing with potential research subjects to recruit, assess eligibility criteria, determine subject availability, assist investigators with obtaining informed consent and coordinate appointments with the recruitment team.* Clinical procedures: venipuncture, vital signs, ECG, spirometry, and procedures as dictated by study protocol.