Job Description

At K2 Medical Research, a privately-owned clinical research facility in the greater Orlando and Central Florida area, we specialize in conducting multiphasic clinical trials that promote the development of innovative and effective medical treatments while maintaining the safety and privacy of our participants. We are committed to fighting the diseases that plague our loved ones and ourselves. By harnessing the power of advanced clinical research and connecting our patients with the treatments of tomorrow, we can improve the health of our local communities, and by extent, the population of our world.

K2 has an exciting opportunity for a Principal Investigator, a license MD or DO, to support a new clinical research initiative in Maitland, FL. This position offers an incredible chance to lead studies that will contribute to advancing our understanding of neurodegenerative diseases and other diseases, providing valuable experience in both research and patient care. K2 Medical Research is committed to fostering a collaborative and supportive environment, where new investigators can thrive and make significant contributions to the field. 

The Medical Doctor (PI) promotes Good Clinical Practice in the conduct of clinical investigations by ensuring adherence to protocol requirements, protecting the rights and welfare of study subjects, assuring the integrity of data generated at the site and directing the conduct of the clinical investigation according to federal and state regulations and guidance documents.

Primary Responsibilities:

• The PI assumes full responsibility for a clinical trial, including the oversight and ethical conduct of the study, 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 Sponsor, CRO and Site
• Evaluate patient eligibility for a clinical trial as per protocol
• Review and discuss study protocols and obtain (or delegate) informed consents 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 all safety variables, including adverse events, laboratory abnormalities, changes in patient medical status, evaluation of prescribed concomitant medications as per protocol, and un-blinding requests
• Use proper medical judgment in the interpretation and decision-making as it relates to the investigational study
• Review, approve and ensure timely reporting of eCRFs, protocol deviations 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 FDA, IRB, Sponsors, CROs, or their delegated representatives 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
• Review and approve Clinical Study Agreements
• Work with Sub-investigator(s), Clinical Research Coordinators, and key study personnel in overseeing the execution of study protocols 
•  Other duties as assigned

Knowledge, Skills, Abilities:

•  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

Qualifications:

• Medical Degree and broad-based post-graduate experience
• Board certification in Neurology or Gerontology preferred; or family physician or Internal medicine
• Medical License within the State of Florida
• A minimum of 3 or more years of experience in a clinical research position (Preferred)
• Principal Investigator of Clinical Trials: 3 years (Preferred)

At K2, we value our employees and their professional and personal needs, and support these through our benefit offerings:

• Medical, Dental, Vision, Flexible Spending Accounts, Employer paid Long-Term disability and Life Insurance, Short Term Disability, Accident and Critical Illness Insurance, Voluntary Life and Long-Term Care Insurance, Legal Shield, Employee Assistance Program, and various discount programs.
• 401(K) Plans- Traditional and Roth plans are available; 4% employer match that is immediately vested
• PTO of 16 days per year, 17 days after the first year of FT employment
• 9 paid Holidays
• K2 observes a four-day work week, Monday through Thursday, for full time employees. Fridays are non-working days unless required by business needs. 

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