Geriatrician - Principal Investigator

Pinnacle Clinical Research

$150K — $200K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 1-2 years of clinical experience in Geriatrics.
  • Experience with the aging population in clinical or research environments.
  • Clinical research experience preferred but not mandatory.
  • Current physician license required.
  • Board Certified in Geriatric medicine.

Responsibilities

  • Review and understand study-related activities and protocols.
  • Assume responsibilities as an Investigator according to FDA regulations.
  • Adhere to all study protocols and Good Clinical Practices (GCP).
  • Maintain confidentiality regarding sponsors and clinical trials.
  • Perform various study-related procedures including physical exams and patient assessments.
  • Assist in preparation for monitoring visits.
  • Handle subject recruitment and screening procedures.
  • Provide weekend and after-hours coverage as needed.

Benefits

  • Flexible working arrangements.
  • Opportunity to collaborate in pioneering medical research.
  • Engagement in impactful work that contributes to patient care advancement.
  • Professional development opportunities within a leading clinical research network.
Full Job Description
Summary: Pinnacle Clinical Research is seeking a Full-time Geriatrician 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 and steatotic liver disease with 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.


Duties and Responsibilities:

  • Review and hold expert knowledge of study-related activities and protocols.
  • Assume all responsibilities and obligations as an Investigator, 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.


Qualifications:

  • At least one to two years of clinical practice in Geriatrics.
  • Experience working with an aging population in a clinical or research setting.
  • Clinical research experience is preferred but not required.


Knowledge, Skills, and Other Abilities:

  • 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.


Competencies:

  • 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 Foxfire, and web-based enterprise solutions software.


Certificates and Licenses:

  • Current physician license.
  • Board Certified in Geriatric medicine.


FLSA Classification: This is an exempt position.

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.

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