Pinnacle Clinical Research
The Principal Investigator (PI) will oversee and conduct clinical trial research activities, ensuring compliance with protocols, regulations, and ethical guidelines. The role includes providing clinical oversight, monitoring patient safety, and collaborating with research staff to advance clinical studies, with a focus on patients with Alzheimer’s dementia.
Key Responsibilities
- • Personally conduct or supervise the research.
- • Ensure that each individual to whom a task is delegated is qualified by education, training, and experience to perform each of their delegated tasks.
- • Protect the rights, safety, and welfare of the participants who will be in their care.
- • Ensure research is conducted in accordance with all federal regulatory requirements, state law, and Pinnacle Clinical Research policies (including SOPs).
- • Ensure research is conducted in accordance with the IRB-approved plan.
- • Ensure the accuracy, security, and integrity of the research data and the subsequent analysis of that data.
- • Review and hold expert knowledge of study-related activities and protocols.
- • Assume all responsibilities and obligations as an Investigational, per Title 21 part 312 and FDA Form 1572.
- • Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times.
- • Maintain study sponsor and clinical trial confidentiality.
- • Perform study-related procedures such as physical examinations, informed consent, subject history, adverse events, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessments.
- • Review and adjudicate all lab, imaging, and biopsy findings.
- • Assist in the preparation for study monitor visits.
- • Perform subject screening and recruitment.
- • Provide some weekend coverage to facilitate study visits by protocol.
- • Provide after-hours phone call coverage as needed.
Required
- • At least one to two years of clinical practice in Neurology or Geriatrics.
- • Experience working with an aging population in a clinical or research setting.
- • Current Texas physician license.
- • Board Certified in Neurology, Geriatric, or a subspecialty.
Preferred
- • Alzheimer's Disease research experience is highly preferred.
- • Clinical research experience is preferred but not required.
- • Bilingual (English and Spanish) strongly preferred.
Summary: Pinnacle Clinical Research is seeking a part-time or full-time Neurologist (preferably behavioral), Geriatrician, or Psychiatrist to serve as a Principal Investigator (PI) for clinical trials. The PI will oversee and conduct research activities, ensuring compliance with protocols, regulations, and ethical guidelines. Responsibilities include providing clinical oversight, monitoring patient safety, and collaborating with research staff to advance clinical studies. Ideal candidates will have significant experience in caring for patients with Alzheimer’s dementia, strong analytical skills, and a dedication to advancing clinical research through high-quality patient care and ethical study practices.
The PI agrees to assume the overall responsibility for the study's conduct. By doing so, the User inherently agrees to:
- Personally conduct or supervise the research.
- Ensure that each individual to whom a task is delegated is qualified by education, training, and experience to perform each of their delegated tasks.
- Protect the rights, safety, and welfare of the participants who will be in their care. To do this, they agree that the research:
- Is conducted in accordance with all federal regulatory requirements, state law, and Pinnacle Clinical Research policies (including SOPs).
- Is conducted in accordance with the IRB-approved plan.
- They will ensure the accuracy, security, and integrity of the research data and the subsequent analysis of that data.
- Review and hold expert knowledge of study-related activities and protocols.
- Assume all responsibilities and obligations as an Investigational, per Title 21 part 312 and FDA Form 1572.
- Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times.
- Maintain study sponsor and clinical trial confidentiality.
- Perform study-related procedures such as physical examinations, informed consent, subject history, adverse events, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessments. Review and adjudicate all lab, imaging, and biopsy findings.
- Assists in the preparation for study monitor visits.
- Perform subject screening and recruitment.
- Provide some weekend coverage to facilitate study visits by protocol.
- Provides after-hours phone call coverage as needed.
- Alzheimer's Disease research experience is highly preferred.
- At least one to two years of clinical practice in Neurology or Geriatrics.
- Experience working with an aging population in a clinical or research setting.
- Clinical research experience is preferred but not required.
- Bilingual (English and Spanish) strongly preferred.
- Possess impeccable integrity and personal and professional values that are consistent with PCR’s high standards and mission.
- Comply with the company policies, code of ethics, and guiding values always.
- Must be able to work independently and collaborate with a team.
- Excellent written and oral communication skills.
- Organizational skills.
- Ability to pay attention to detail.
- People skills, including possessing a positive, friendly, and professional demeanor.
- Ability to be flexible with changing priorities.
- Ability to communicate in a diplomatic and professional manner.
- Strong interpersonal skills.
- Excellent computer skills.
- Knowledge of Microsoft Office, Internet Explorer, Google Chrome, Mozilla Firefox, and web-based enterprise solutions software.
- Current Texas physician license.
- Board Certified in Neurology, Geriatric, or a subspecialty.
Work Environment And Physical Demands
The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
- Work may be performed in an office/laboratory and/or a clinical environment.
- Occasional travel may be required, domestic and/or international 10%.
- Ability to work in an upright and/or stationary position for 6-10 hours per day.
- Frequent mobility is required.
- Occasionally squatting, kneeling, or bending.
- Light to moderate lifting and carrying (or otherwise moving) objects, including medical equipment, with a maximum lift of 20-50 lbs.
About Pinnacle Clinical Research
Pinnacle Clinical Research Network provides world-class clinical trial solutions to its member sites, sponsors, CROs, researchers and patients to accelerate the results of their trials. By advocating for quality, integrity and diversity in clinical research data, Pinnacle is dedicated to advancing unmet areas of medical research and leading pivotal scientific discoveries.
Keep track of your job search
Save personal notes for each job to track your thoughts, application status, and follow-ups.
Try for freeUpload your resume
Sign up to upload your resume and get AI-powered customization for job applications.
Sign up freePractice your interview
Get AI-powered mock interviews tailored to this Behavioral Neurologist/Geriatrician - Principal Investigator role. Upload your resume and practice with real-time voice feedback.
Sign up to practice