An open, fully funded position for a research assistant is available in the Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases at the University of Texas Health San Antonio (UTHSA) (https://biggsinstitute.org/). We are looking for an exceptional candidate with expertise in clinical research to join a collaborative team of clinicians, sponsors, and research team members conducting state-of-the art research studies to understand familial genetics underlying dementia, diagnose chronic traumatic encephalopathy in former football players, and other ongoing studies focused on dementia.

• High attention to detail and strong organizational skills.

• Excellent written and verbal communication skills.

• Ability to work well independently with research participants, clinicians, and staff with minimal supervision.

• Possess strong skills for multitasking, meeting competing deadlines, prioritizing and supporting the investigator team.

Education:

• Bachelor’s degree in basic science is required.

Experience:

• No experience is required.

Preferred:

• Bilingual in English/Spanish is highly preferred.

• Supports the investigative team in the planning, evaluation, implementation, and documentation of research studies.

• Maintains research databases; prepares and submits individual study progress reports as needed.

• Actively recruits, screens, enrolls, and schedules participant for various industry-sponsored or investigator-initiated trials.

• Schedules, coordinates, and confirms study visits.
• Obtains informed consent of study participants and ensures participant understanding and assessing willingness to continue with the study at each visit.
• Completes screening procedures for the review of the investigative team, conducts study visits, collects and processes data collection, completes research related forms, completes electronic data entry, and maintains study subject data and upload of source documents for various studies.

• Ensures compliance with all regulatory agencies and funding source, Maintenance of appropriate regulatory files in compliance with ICH/GCP.

• Coordinates the interim monitoring visits for source document verification as well as preparing/updating IRB submissions to central and local IRBs.

• Assists in conducting a variety of research projects of limited complexity, collecting, evaluating, and interpreting data

• Follow industry standards and safety regulations.
• Maintains excellent communication with the investigative team.

• Performs all other duties as assigned.