What are the responsibilities and job description for the Physician/Medical Director: Principal Investigator at Clinical Research Site position at Noble Clinical Research, LLC?
Noble Clinical Research, one of Tucson's oldest dedicated clinical trials sites, is looking for a Medical Doctor who can become a Principal Investigator on FDA-supervised industry-sponsored clinical trials.
This job requires an MD or DO, a valid Arizona medical license, and board certification or eligibility in a generalist specialty, such as family medicine, internal medicine, or geriatrics.
Prior clinical research experience is greatly appreciated, but we can rapidly bring a dedicated candidate without prior clinical research experience up to speed.
Many doctors find that working in clinical research is much easier than working at a traditional clinic, for the following reasons:
- Patient throughput is much lower. Even on a busy day, you usually will not see more than 15 patients.
- You do not have the stress of having to diagnose or treat any health condition. You only have to follow the research protocol.
- Patients are not afraid of a diagnosis. They have already been diagnosed with any health condition they may have; they are now optimistic about getting free potential access to next-generation, investigational therapies
However, in the spirit of balance, we will note the following differences from a traditional care setting that some doctors find too different:
- There is a lot more paperwork in clinical research than in traditional medicine.
- Our office uses paper charts/paper source rather than Electronic Medical Records (still permitted on clinical trials).
- There is somewhat less patient interaction on a clinical research study than in a traditional clinic, but it is less rushed, and you are welcome to offer patients advice and testing outside of the clinical trial.
We can offer a range of hours, depending on your personal preferences and schedule.
We acquire new clinical trials on a monthly basis, but currently we have trials in the following indications:
- Moderate-to-severe COPD
- Moderate-to-severe asthma
- Moderate-to-severe plaque psoriasis
- Vitiligo
- Eczema
- Major Depressive Disorder
- Sleep apnea
- Shift-work sleep disorder
Responsibilities
- Oversee and manage clinical trials, ensuring compliance with FDA regulations and ethical standards.
- Maintain accurate medical records and ensure adherence to HIPAA regulations.
- Adhere to the specific protocol for each research study--you will be thoroughly trained on each one.
Qualifications
- Valid Arizona medical license
- MD or DO degree
- Board certification (or eligibility) in: family medicine, internal medicine, or geriatrics
- Prior experience in clinical research as a sub-investigator or principal investigator is appreciated but not required.
Job Type: Contract
Pay: $125.00 - $200.00 per hour
Expected hours: 4 – 25 per week
Benefits:
- 401(k)
- Flexible schedule
- Professional development assistance
- Referral program
- Relocation assistance
Schedule:
- 4 hour shift
- Choose your own hours
- Day shift
- Monday to Friday
- No nights
- No weekends
Supplemental Pay:
- Bonus opportunities
Application Question(s):
- Please share your board certifications or specialties.
License/Certification:
- Medical License (Required)
Ability to Relocate:
- Tucson, AZ: Relocate before starting work (Required)
Work Location: In person
Salary : $125 - $200