This job is archived
Principal Investigator
Sarasota, Florida, United States
Job Summary
Occupation
Physician
Specialty
Gastroenterology
Degree Required
MD/DO
Position Type
Permanent/Full-Time
Work Environment
Academic/Training Program
Clinic/Private Practice
Location
Florida, United States
Visa Sponsorship
No
Job Description
Last Update:
4/27/20
Lead a research facility with a team of more than 20 healthcare professionals. Florida Research Institute is a multi-therapeutic, dedicated clinical research site with an industry track record of providing high performance rates and quality data.
We are searching for a principal investigator to apply medical knowledge/experience to oversee and direct the clinical course of research participants in clinical trials. The person in this role must have a thorough knowledge of clinical trial management and monitoring, as they will be responsible for working with the sub investigator in overseeing the execution of study protocols, delegating study-related duties to site staff and ensuring site compliance with study protocols and other state/local regulations as applicable.
The principal investigator will also help assess physical health and administer treatments throughout the study aligned with scope of practice delegated responsibilities. Additionally, they will oversee study conduct and assure study participant safety.
We are searching for a principal investigator to apply medical knowledge/experience to oversee and direct the clinical course of research participants in clinical trials. The person in this role must have a thorough knowledge of clinical trial management and monitoring, as they will be responsible for working with the sub investigator in overseeing the execution of study protocols, delegating study-related duties to site staff and ensuring site compliance with study protocols and other state/local regulations as applicable.
The principal investigator will also help assess physical health and administer treatments throughout the study aligned with scope of practice delegated responsibilities. Additionally, they will oversee study conduct and assure study participant safety.
Duties include but are not limited to:
- Ensure the safety of study participants, and maintain communication with patients, FRI team members and clinicians.
- Provide clinical and medical support and oversight for research clinical trials based on scope of practice.
- Collaborate with clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols.
- Assess, grade, and document adverse events; apply triage and judgment to determine course of action.
- Oversee and, as needed, administer medications and treatments per study protocol and scope of practice.
- Comply with institutional policies, standard operating procedures, and guidelines; prepare and submit documentation as required by the study protocol and study sponsor; interpret complex protocols.
- Identify, recruit, and enroll study participants, as well as maintain study participant records; determine study participant criteria.
- Support sponsor investigator research with investigational new drug/investigational device exemption applications.