What are the responsibilities and job description for the Psychiatrist position at SQRL?
Highlights:
- Part time schedule, add the work to your existing practice or career
- Stepping stone into clinical research - a field notoriously difficult to break into!
- Take part in creating life changing medications and therapies
The Company:
Our client is a fast growing clinical research site network that started in 2015 and grew to 11 sites with plans to double in the next couple years! They have run many clinical studies in Phase I - IV in therapeutic areas mainly focused in GI, Hepatology, and CNS! Their goal is to be the best place to work in the country, and they are excited to find people excited to make that vision come to life through quality patient care and research.
Job Description
As a Psychiatrist, you will aid in the execution of psychiatric and CNS clinical trials to test new medications. You will promote Good Clinical Practice, integrity of data generated at the site, and directing the conduct of the Clinical Investigation per guidelines and sponsors. You will also work collaboratively with the study team and regulatory personnel to ensure the welfare of study participants, oversee the execution of study protocol, delegate study related duties, and ensure site compliance with study protocols, laboratory procedures, and standards.
- Provide Sponsor and IRB with documentation of credentials as required.
- Evaluate and screen potential subjects based on study eligibility criteria and perform psychiatric evaluations.
- Perform assessments as a part of clinical study procedures.
- Provide ongoing assessments of study subjects including any potential adverse events, or serious adverse events
- Provide medical management of Adverse Events and emergent events
- Perform and review psychiatric ratings performed by raters in accordance with the clinical study protocol.
- Complete all documentation, paper and electronic, as required per protocol
- Provide oversight and ensures proper delegation of duties to appropriate staff
- Provide and maintain updated study related documentation as required by the clinical research trial to ensure data integrity.
- Evaluate and report safety reports, protocol noncompliance and any other protocol specific reports.
- Ensure compliance with legal issues including but not limited to patient confidentiality and risk management; ensures compliance with federal, state and local regulations.
Qualifications:
- Board Certification in Psychiatry
- Active license to practice medicine in the state of Florida (or ability to obtain one after receiving an offer)
- Ability to work on part time in Maitland, FL
