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Clinical Research Director Assistant

General Dynamics Information Technology
USA TX Lackland AFB - Lackland AFB (TXC010), United Statesfull_timeVerifiedPosted 19 Sept 2024
💰 $69,000/yr($60,549/yr$69,000/yr)

About the role

Type of Requisition:

Regular

Clearance Level Must Currently Possess:

None

Clearance Level Must Be Able to Obtain:

None

Suitability:

Public Trust/Other Required:

NACI (T1)

Job Family:

Program Management

Job Qualifications:

Skills:

Clinical Research, IRB (Inactive), Researching

Certifications:

Experience:

5 + years of related experience

US Citizenship Required:

Yes

Job Description:

GDIT's Military Health Team is hiring a Clinical Research Director Assistant to support the 59th Medical Wing located at Lackland Airforce Base in San Antonio, TX.

The 59th Medical Wing Science and Technology (ST) office advises and conducts clinical and translational research on matters pertaining to the medical aspects of the Air Expeditionary Force and the health of Air Force (AF) personnel and beneficiaries. In order to support the required research, ST offices conduct translational research in the areas of emergency medical care, combat casualty care, force health protection, restorative medicine, clinical and rehabilitative medicine and specialty centers.

Learn More Here --> https://www.59mdw.af.mil/


HOW A PROGRAM ANALYST WILL MAKE AN IMPACT

  • Assists in institutional research for the 59th Medical Wing.
  • Assists in operations of the IRB and preparing protocols to go through the board process.
  • Works with investigators in preparing and reviewing protocols ensuring protocols meet all applicable Air Force, DoD, and Federal requirements.
  • Manages data collection and analysis and oversees the formulation of research reports (i.e., reports to higher headquarters, accrediting agencies, research partners, etc.)
  • Assists presiding member of the Wilford Hall Medical Center IRB to develop processes to review and coordinate all research protocols in accordance with the Common Rule, Belmont Report, and other federal, DoD and AF regulations.
  • Assists in developing and writing operating instructions for all processes associated with performing research within the institutions.  Acts as an appointed non-voting member of the IRB.
  • Determines category of IRB approval required for studies submitted.
  • Assists in preparing IRB agenda working with the IRB Presiding Member and IRB protocol staff and publishes agenda.
  • Assists in tracking all ongoing approval and concurrence actions from Higher Headquarters and coordinates actions with principle investigators, IRB members, and Division personnel.
  • Assists in controlling protocol documentation, establishing suspense’s and ensuring documentation is complete and prepared for scheduled IRB meetings.
  • Assists in completion and review of IRB minutes, reviewing for completeness and thoroughness prior to submission for signature and coordination with higher headquarters review. Assists in ensuring minutes contain all pertinent information relevant to risk determination and regulatory compliance to expedite review by outside compliance agencies.
  • Assists in tracking training and compliance issues of all individual investigators involved in research in the 59th Medical Wing, ensuring appropriate training is completed as required and that a;; personnel meet compliance regulations pertaining to research being conducted within the control of the WHMC IRB.
  • Assist IRB Chair and Presiding Official in conducting meetings ensuring required members are available, votes are cast and conflict of interest issues are resolved in accordance with commonly accepted rules of order.
  • Review protocol changes submitted to the IRB required changes and assists in approval and concurrence actions from the Air Force Surgeon General's Office.


WHAT YOU’LL NEED TO SUCCEED:

  • Bachelor of Science Degree with 5+ years of experience in clinical research or a Master’s/PhD in scientific field with 2+ years.
  • Documented authorship of scientific publications, conducting clinical research to include experience in developing and designing research protocols or experience with research compliance and auditing is required.
  • Experience and broad knowledge of medical, nursing or allied health care fields used to interpret research functions.
  • Working general

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Company

General Dynamics Information Technology

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