SQRL
Highlights
- No research experience needed! Training provided!
- As needed, highly part time position with occasional on site work in Utah
- Research Study Profit Model - the more the studies make, the more you make!
- Open to a wide variety of board certified physicians!
The Company
Our client is a clinical research company and biobank excited to expand their research to more sites within the US! They pride themselves on their data-driven healthcare platform and AI tools that they use to transform treatment of chronic illnesses. What makes their biobank unique is it's speciality focus, specifically for chronic conditions and rare disease.
The Role
As a Principal Investigator you will be responsible for oversight and execution of clinical trials that test new medications on the behalf of sponsor/pharmaceutical companies. You will work a hybrid model, ensuring Good Clinical Practice and following research protocols.
- 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.
- Travel to the site location for occasional on site requirements
Qualifications:
- Education: MD/DO
- Board certification
- Specialty including: Cardiology, GI, Rheumatology, Immunology, Neruology, and Rare Disease
- Ability to work on site at least 1 time per month (travel from out of state is reimbursed as needed)