Clinical Research Student Assistant: Gurnett Lab
About The Position
Participates in research activities which may include: subject recruitment, confirmation of subject eligibility, informed consent process, completion of case report forms, data clarification, IRB preparations, chart abstraction. Adheres to approved recruitment & enrollment strategies. Maintains regulatory documents per the established protocol or sponsor requirements. Creates/reviews source documents and sets up study files. Ensures compliance with protocol guidelines and requirements of regulatory agencies. Analyzes data through the use of memos, coding and qualitative analytic software. Assists in the preparation of reports and professional research papers. Assists in preparation of materials to submit for IRB approval. Renders age appropriate care & services based on the patient and/or their developmental needs.
Requirements
- High School Diploma / GED
- Enrollment in school
- Internships or paid experiences coordinating research study activities varying size and complexity
- Several internships or paid experiences coordinating research study activities varying size and complexity
- Good written and verbal communication skills
- Able to work in an organized fashion, work well with others
- Good attention to detail
- Fully trained on good clinical practices (GCP) and regulatory responsibilities
- Knowledgeable of IRB, FDA, ICH, GCP, or other sources
- Demonstrates the knowledge & ability to render age appropriate care & services based on the patient and/or their developmental needs
Nice To Haves
- Bachelor's Degree
- Pediatric clinical research experience
- Proficiency with Microsoft Office applications desirable
Responsibilities
- Subject recruitment
- Confirmation of subject eligibility
- Informed consent process
- Completion of case report forms
- Data clarification
- IRB preparations
- Chart abstraction
- Adheres to approved recruitment & enrollment strategies
- Maintains regulatory documents per the established protocol or sponsor requirements
- Creates/reviews source documents and sets up study files
- Ensure compliance with protocol guidelines and requirements of regulatory agencies
- Analyzes data through the use of memos, coding and qualitative analytic software
- Assist in the preparation of reports and professional research papers
- Assist in preparation of materials to submit for IRB approval
- Renders age appropriate care & services based on the patient and/or their developmental needs
Benefits
- Annual influenza vaccine
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Education Level
High school or GED
