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Related keywords
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Research Administrative Assistant Jobs
Company | Urology San Antonio |
Address | San Antonio, TX, United States |
Employment type | FULL_TIME |
Salary | |
Category | Medical Practices |
Expires | 2023-09-15 |
Posted at | 8 months ago |
Job Summary
- Prints protocol mailings and safety reports and distribute the information to the Clinical Research Supervisor in a timely manner.
- Assists with coordination and communications of research projects per the funding agency's award statement. This process includes the recruitment of participants and the implementation of all aspects of study protocols.
- Provides supports with writing procedure sheets for research protocols along with developing datasheets and other research-related forms.
- Participates in the training of new staff, students, and volunteers on all aspects of the research protocols.
- Obtains and track medical records for research subjects.
- Takes part in developing databases and tracking data.
- Interviews potential participants and maintain clinic schedules
- Helps the Research Team with subject recruitment activities (mailings, posting fliers, contacting outside agencies, etc.)
- Assists with the acquisition and maintenance of all data collected for research studies.
- Assists with telephone screenings and schedule research subjects for evaluations to include maintaining the schedule for research appointments.
- Supports clinical research studies by collaborating with research participants at Urology San Antonio and interacts with patients and their families.
- Creates protocol charts for CRA's and assists in entering and maintaining information in the Clinical Trials Management System.
- Answers the Research department's main phone line and directing calls to the appropriate staff.
- Stress Management/Composure
- Initiative
- Ethical Conduct
- Flexibility
- Personal Effectiveness/Credibility
- Patient & Customer Focus
- High School diploma or General Educational Development (GED)
- Keen attention to details
- Experience managing operations (coordinating/scheduling patient visits)
- Maintain confidentiality
- Ability to work well independently
- Experience with Microsoft Office Suite (Outlook, Word, Excel, PowerPoint)
- Ability to adjust to consistent change, effectively and efficiently
- Possess strong skills for multitasking, meeting competing deadlines, prioritizing, and supporting PIs for multiple projects
- Clinical research certification a plus but not required
- Clerical and computer experience preferred, experience in medical setting a plus.
- Excellent written and verbal communication skills
- Adept at creative problem-solving
- Great attention to detail and strong organizational skills
- Positive attitude
- Bilingual/Spanish
- HIPAA compliance
- College Degree in the field of Science
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