The Company
Our client is a fast growing site network that currently has over 10 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: GI, Liver disease, memory care, general medicine, and more. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors.
The Role
The Sub-Investigator (Clinical Research NP) is responsible for oversight and execution of clinical trials that test new medications on the behalf of sponsor/pharmaceutical companies! You will work in a clinic to promote Good Clinical Practice and follow research protocols assigned. This includes things like medical management of patients on trial, administering medications, documentation, tracking and management of adverse events, and overall management of the study. You will work along a Principal Investigator, have a team of skilled coordinators, managers, and assistants as well!
- Evaluate and screen potential subjects based on study eligibility criteria
- Perform and review medical procedures in accordance with the clinical study protocol
- Complete all documentation, paper and electronic
- Provide oversight and ensures proper delegation of duties to appropriate staff
- Provide and maintain updated study related documentation
- Evaluate and report safety reports, protocol noncompliance and any other protocol specific reports.
Qualifications
- Nurse Practitioner or Physician Assistant
- Ability to dedicate a full time schedule on site in Maitland, FL
- Experience with Clinical Research Studies preferred
