"Neuropsychology Research Assistant"

A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.

The emphasis of this research position is on the administration of standardized cognitive assessments and research measures for clinical research studies examining cognitive functioning in neurological and medical conditions. The successful candidate will work closely with faculty and research staff to support study operations, including participant coordination, cognitive testing, and data collection. The role involves assisting with in person research visits, administering computerized and tablet based assessments, supporting EEG based research procedures, and maintaining accurate research documentation and databases. The candidate is expected to work in a semi independent manner while following established research protocols and regulatory requirements to assist in clinical research and related projects.

Characteristic Duties and Responsibilities:

Knowledge of all 8 competency domains is expected:

1. Scientific Concepts and Research Design
2. Ethical Participant Safety Considerations
3. Investigational Products Development and Regulation
4. Clinical Study Operations (GCP's)
5. Study and Site Management
6. Data Management and Informatics
7. Leadership and Professionalism
8. Communication and Teamwork

Position Specific Responsibilities will Include:

• Knowledge across multiple competency domains is expected, including scientific research procedures, ethical conduct of human subjects research, clinical study operations, data management, professionalism, and communication.
• Day to day responsibilities in this role will support multiple aspects of the research process, including:
• Administer standardized cognitive assessments and research instruments to study participants in accordance with established protocols.
• Assist with the implementation of research protocols, including participant recruitment, scheduling, enrollment, informed consent procedures, and completion of research visits.
• Support EEG based research procedures, including equipment setup, task administration, and monitoring of data collection under supervision.
• Administer computerized and tablet based assessments, including standardized cognitive testing platforms.
• Collect, enter, code, and manage research data using approved databases and tracking systems.
• Track data completeness and assist with quality control procedures across study activities.
• Maintain accurate study documentation, regulatory binders, and research logs.
• Assist with study start up and ongoing study maintenance activities as needed.
• Support data management and data processing activities in collaboration with faculty and research staff.
• Assist with preparation of study materials, presentations, and research related documents as requested.
• Assist with completion and maintenance of IRB applications and other regulatory requirements.
• Provide administrative and operational support for research activities, including scheduling meetings and preparing meeting materials.
• Serve as a point of contact for participants and research staff as appropriate.

Required Qualifications:

• High school diploma or GED.
• Experience with or knowledge of human subjects research procedures.
• Ability to administer standardized assessments and follow detailed research protocols.
• Demonstrated organizational skills and attention to detail.
• Ability to accurately collect, enter, and manage research data.
• Basic proficiency with common computer applications, including Microsoft Word, Excel, and other data entry or database systems.
• Strong communication skills and ability to interact professionally with research participants and study staff.
• Ability to work independently while also functioning effectively as part of a research team.
• Willingness to learn new research procedures, assessment tools, and data management systems.
• Ability to maintain confidentiality and comply with ethical and regulatory requirements related to clinical research.

Preferred Qualifications:

• Bachelor's degree in psychology, neuroscience, health sciences, or a related field.
• Experience with or knowledge of human subjects research procedures.
• Ability to administer standardized assessments and follow detailed research protocols.
• Demonstrated organizational skills and strong attention to detail.
• Ability to accurately collect, enter, and manage research data.
• Proficiency with common computer applications, including Microsoft Word, Excel, and other data entry or database systems.
• Strong communication skills and ability to interact professionally with research participants and study staff.
• Ability to work independently while also functioning effectively as part of a research team.
• Willingness to learn new research procedures, assessment tools, and data management systems.
• Ability to maintain confidentiality and comply with ethical and regulatory requirements related to clinical research.

This is a part time, 12 hours a week position.

The work schedule is Tuesdays 9 AM - 5PM and Fridays 9 AM - 1 PM.