Clinical Research Physicians (Pooling)

K2 Staffing LLC•Berry Hill, TN

3d•Onsite

About The Position

At K2 Medical Research, we are transforming healthcare by delivering tomorrow’s treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we lead multiphasic trials in therapeutic areas ranging from neurodegenerative to cardiometabolic medicine. Our culture is grounded in clinical excellence and a patient-first mission. We are seeking mission-driven individuals ready to play a meaningful role in bringing life-changing treatments to the patients who need them most. K2 is seeking experienced Physicians to provide additional support to our clinic in Nashville, TN in an onsite and full-time capacity. This PI should be Board-certified in the state of Tennessee. With leadership that has been in clinical research for the past 20+ years, K2 has a strong reputation in the drug development industry. Our clinical trials experience/therapeutic areas include neurodegenerative disorders (Alzheimer’s, Parkinson’s, LBD), general medicine and some psychiatry as well. We have taken part in clinical trials for all current FDA-approved therapies that slow the progression of Alzheimer’s disease (AD) 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 to practice your best medicine. You will work as part of a team of dedicated researchers, including nurses and research coordinators.

Requirements

Clinical Research experience is required.
Must be Board Certified in certain specialties (Family Practice, Internal Medicine, Neurology, Psychiatry), Emergency Medicine)
Must have a current UNRESTRICTED TN medical license and geographic location highly desired.
Broad knowledge of general medicine
Strong analytical and problem-solving skills
Excellent organizational skills, detail oriented, efficient, and able to multi-task and prioritize effectively
Excellent interpersonal skills
Strong written and verbal communication skills

Responsibilities

Responsibly and ethically provide medical oversight to the research team and research patients
Review patient eligibility for clinical trials
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, etc.
Use proper medical judgment
Ensure accurate documentation
Review and discuss any medical or protocol-related concerns with medical team
Maintain compliance with GCP and all assigned trainings
Attend study-related meetings (occasional travel to exciting cities!)
Work with other physicians, nurses, and key study personnel in overseeing the execution of study protocols
Other duties as assigned