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Physician Assistant - Sealy Institute for Vaccine Services - Operations Research
Physician Assistant - Sealy Institute for Vaccine Services - Operations Research-April 2024
League City
Apr 1, 2026
About Physician Assistant - Sealy Institute for Vaccine Services - Operations Research

  Physician Assistant - Sealy Institute for Vaccine Services - Operations Research

  League City, Texas, United States

  Patient Care

  UTMB Health

  Requisition # 2400007

  JOB SUMMARY

  To provide patient care assistance in a clinic setting in one or more specialized areas, under the supervision of a primary care physician.

  EDUCATION & EXPERIENCE

  Minimum Qualifications:

  Completion of a physician assistant program accredited by the Accreditation Review Commission on Education for the Physician Assistant (ARC-PA)

  No experience required

  LICENSES, REGISTRATIONS OR CERTIFICATIONS

  Required:

  Certification by the National Commission on Certification of Physician Assistants (NCCPA)

  Licensed Physician Assistant by the Texas Physician Assistant Board/Texas Medical Board (TPAB/TMB)

  Current students who have not yet completed their physician assistant program or recent graduates who have not yet obtained their NCCPA certification or TPAB/TMB physician assistant license are eligible to apply for this position. However, official employment is contingent upon the successful completion of an accredited physician assistant program, NCCPA certification and TPAB/TMB physician assistant licensure.

  JOB DUTIES:

  Completes all required training/certification

  Reviews goals and requirements of new and on-going protocols

  Conducts clinical research, as delegated by Principal Investigator (PI), according to the protocol, local and state regulations, FDA and ICH guidelines, and other regulatory agencies

  Clinical duties to include, but not limited to: obtaining and documenting informed consent, obtaining medical histories, reviewing medications, performing physical exams, ordering and interpreting lab tests and EKGs in collaboration with PI, ordering and dispensing of investigational product, monitoring and assessment of protocol compliance and adverse events, and providing patients with test results and referrals.

  Recruits, screens, and enrolls participants

  Monitors research subjects and provides medical care as necessary

  Plans and designs source documentation for protocols, prepares IRB and regulatory documents; under direction of PI may draft various communications with Sponsors

  Participates in the revision, development and implementation of study-related documents/tools

  Ensures accurate source documentation and completion of appropriate forms as per protocol, monitoring documentation for quality and accuracy

  Performs Quality Management activities as assigned

  Monitors enrollment goals and modifies recruitment strategies, as necessary

  Identifies and facilitates process changes as appropriate

  Responsible for internal and external quality assurance; ensures the development of an ongoing productive relationship with the study monitor

  Attends required clinical research staff meetings

  Adheres to internal controls established for department.Performs other related duties as required.

  Equal Employment Opportunity

  UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a VEVRAA Federal Contractor, UTMB Health takes affirmative action to hire and advance women, minorities, protected veterans and individuals with disabilities.

  Compensation

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