Principal Investigator (Internal Medicine)

Position Overview: We are seeking a highly skilled and experienced Principal Investigator medical physician to join our team. As the Principal Investigator, you will be responsible for oversight of all clinical trial studies according to study protocols, company processes and GCP.

This is a part-time position with flexible hours, ranging from 20 to 30 hours per week. The exact hours will vary based on the needs of the clinical trial study, offering both adaptability and the opportunity to work on a dynamic and engaging project.

• Oversee site personnel in the execution and delivery of safe trial practices.
• Review and report on screening failures, safety and participant retention rates.
• Oversee clinical evaluation and assessments of clinical trial studies.
• Interface with IRBs and study Sponsors on a regular basis.
• Comply with all medical duties per study protocols, SOP, GCP and state regulations.
• Collect and analyze data to identify patterns or trends of the clinical trials.
• Prepare detailed reports documenting findings and recommendations for improvement.
• Stay up-to-date with the latest developments in SOPs and documentation requirements.

Qualifications:
- Active and unrestricted Medical License - California.

• 2 years experience as a Principal Investigator of Sub-Investigator, preferred. Although we are willing to train the right candidate.
• Strong analytical skills with the ability to collect, analyze, and interpret complex data.
• Excellent written and verbal communication skills for report writing and presenting findings
• Ability to effectively manage a team and prioritize tasks in a fast-paced environment.
• Attention to detail and ability to maintain confidentiality when handling sensitive

Information.

If you are a highly motivated individual with a passion for clinical research, we encourage you to apply for this position.

License/Certification:

• DEA License (Required)
• CA Medical Board Physician's License (Required)