Our Clinical Trials group in Central FL are looking for RN’s to add to their facilities in Daytona Beach FL
Under the direction of the Clinical Trials Manager and the Clinical Trials Site Supervisor, assists in ensuring the integrity and quality of the clinical trial(s) are maintained and conducted in accordance with federal, state, and local regulations, Institutional Review Board (IRB) approvals, policies and procedures.
With the direction of the Principal Investigator (PI), this position coordinates research activities.
Serves as the first point of contact by telephone and mail with the study participants for recruitment, scheduling of visits, protocol adherence and retention.
Travels to other medical office buildings. This position is also responsible for protecting the health, safety, and welfare of clinical trial participants.
Utilizes nursing skills to coordinate research-related activities (e.g., scheduling study visits, assisting with nursing assessments of participants, adverse events, and data collection including laboratory and diagnostic studies).
Manages visits with the sponsoring companies and assists in the initiation of clinical trials.
With direction, participates in training, education, and development activities to improve own knowledge and performance to sustain and enhance professional development in the conduct of clinical trials.
Assist with the study completion, resolution of data queries, data lock, study closeout, and archiving of study files.
Provide regulatory support to ensure proper maintenance and storage of critical documents required to be maintained and provided to the sponsor during the conduct of the trial.
Perform nursing procedures required in the protocol in accordance with the scope of practice and the Georgia State Board of Nursing Standards
Report all protocol violations/deviations and adverse events to the PI in a timely manner to ensure the health, safety and welfare of the participants.
With direction, participate in training, education, and development activities to improve own knowledge and performance to sustain and enhance professional development as a clinical trials nurse participating in the conduct of clinical trials. Work with an assigned mentor on a regular basis for training and resource questions.
Participate as a member of the clinical trials team and attend meetings, as requested.
Attend meetings for protocol training initiated by KP and the Sponsor, as requested.
Pay will be Commensurate with experience