We are looking to hire a dynamic board certified/board eligible Physician (preference given to certain specialties) who is interested in learning and working in clinical research. Prior experience preferred but not necessary as training will be provided.

For over 20 years we have taken part in clinical trials for all current FDA approved therapies that slow the progression of Alzheimer’s Disease and most diagnostics (PET tracers, CSF and Blood Biomarkers) for the diagnosis of AD. Additionally, we are actively testing multiple therapeutics in the pioneering field of AD prevention. This is an exciting field of clinical practice with unlimited opportunities where you can practice your best medicine. Our focus is on AD but as a multi-specialty research center, we also participate in clinical trials for diseases such as diabetes, CVD, OA and many others.

We have a team of dedicated researchers, including nurses and research coordinators. We pride ourselves in our humble, collaborative, ego-free environment.

Primary Responsibilities:

• The PI will responsibly and ethically conducts clinical trials, including providing medical oversight, maintaining integrity of the study design, and direction of the research team to ensure research is conducted in accordance with the local and national laws and regulations, including applicable FDA regulations, GCP, ICH guidelines, HIPAA, and all policies and procedures of the trial Sponsor
• Evaluate and discuss with the PI patient eligibility for a clinical trial as per protocol
• Review and discuss study protocols and obtain informed consent from patients
• Meet with patients during designated study visits to perform assessments, including physical examinations and data collection
• Review and interpret laboratory results, EKGs and other diagnostic and safety assessments as required per study protocol
• Monitor safety variables, including adverse events, laboratory abnormalities, changes in patient medical status, evaluation of prescribed concomitant medications as per protocol
• Use proper medical judgment in the interpretation and decision-making as it relates to the investigational study
• Review, approve and ensure timely reporting of protocol deviations and Adverse Events (AE) and Serious Adverse Events (SAE)
• Ensure accurate documentation of study-related procedures
• Ensure proper use and storage of Investigational Product
• Ensure prompt reporting all unanticipated problems or injuries to IRB, Sponsor, or delegated representative
• Meet with trial stakeholders as needed throughout the study
• Review and discuss any medical or protocol-related concerns with medical monitors
• Attend Investigator Meetings and other study-related meetings
• Work with Sub-investigator(s), Clinical Research Coordinators, and key study personnel in overseeing the execution of study protocols
• Other duties as assigned

Qualifications:

• Must be BE/BC
• Must have an unrestricted TN medical license and geographic location
• Willing to work full time, although part time may be a possibility
• Prior Alzheimer's Disease experience preferred but not required