Principal Investigator - Clinical Trials

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 5 to 20 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.

Responsibilities:

• Ensure the medical safety of study participants.
• 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.
  
• 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.