Program Support Assistant

US-Department-of-Veterans-Affair; Dayton (OH); On-site; USD 20,000 - 30,000; Part time

Job summary

U.S. Department of Veterans Affairs in Dayton, OH, is seeking a part-time Research Assistant (Program Support Assistant) to support the day-to-day operations of clinical studies at the Dayton VA Medical Center.

The role involves enrolling participants, collecting data, and assisting the Research Coordinator and Local Site Investigator while ensuring compliance with study protocols and procedures.

Qualifications

• Specialized experience in administrative and program support related to clinical research, including enrollment, data collection, and maintaining research records.

Responsibilities

• Enrolling participants in studies and coordinating study activities.
• Collecting and organizing clinical research data and documentation.
• Providing day-to-day support to the Research Coordinator and Local Site Investigator.

Job description

*** This is a part-time, term-appointed position *** This position is located in the Office of Research and Development (ORD) at Dayton VA medical Center in Dayton, OH. The Program Support Assistant serves as Research Assistant assisting the Research/Study Coordinator with the day-to-day operations of the study including enrolling participants, collecting data, and providing support to the Research Coordinator and Local Site Investigator.

Minimum Requirement:

• Specialized Experience (GS-07): You must have one (1) year of specialized experience that equipped you with the particular knowledge, skills, and abilities (KSA's) to perform successfully the duties of the position, and that is typically in or related to the position to be filled. To be creditable, specialized experience must have been equivalent to at least the next lower grade level (i.e., GS-06). Qualifying specialized experience is experience providing administrative and program support directly related to or in support of human-subjects medical or clinical research studies or programs, including, but not limited to: providing administrative and program support for clinical research activities; collecting and compiling clinical research or study data; maintaining clinical research program records and protocols; coordinating participant and patient activities for clinical research programs including enrollment, scheduling, informed consent processes, and communication; and ensuring activities are conducted in accordance with applicable clinical research protocols, policies, and procedures. (CLEAR DETAILS OF EXPERIENCE REQUIRED: Your resume must show complete information for each job entry, such as beginning and ending dates of employment, duties performed, and/or total hours worked per week.)

For more information on these qualification standards, please visit the United States Office of Personnel Management's website at https://www.opm.gov/policy-data-oversight/classification-qualifications/general-schedule-qualification-standards/.

Experience refers to paid and unpaid experience, including volunteer work done through National Service programs (e.g., Peace Corps, AmeriCorps) and other organizations (e.g., professional; philanthropic; religions; spiritual; community; student; social). Volunteer work helps build critical competencies, knowledge, and skills and can provide valuable training and experience that translates directly to paid employment. You will receive credit for all qualifying experience, including volunteer experience.