The hospital needs to conduct clinical research studies efficiently and accurately.
Requirements
- Electronic data capture system
- Study case report forms
- IRB submission software
- HIPAA compliant documentation
- Study-related technology and equipment
- Biohazardous specimen handling equipment
Responsibilities
- Assist with collection and entry of data into study case report forms and/or electronic data capture system
- Collect and assist with the submission of study related documents, study protocols and study protocol amendments for submission to the IRB
- Maintain accurate and complete documentation of signed informed consent and HIPAA Authorization forms
- Collect, process and ship potentially biohazardous specimens
- Administer structured tests and questionnaires according to research study protocols
- Utilize study-related technology and equipment as part of data collection procedures
- Gather and prepare study-related materials for participants visits
Other
- High School Diploma
- Ability to meet deadlines
- Troubleshoots field issues when necessary
- Detail oriented with high attention to accuracy
- Ability to build rapport, navigate sensitive topics, and maintain confidentiality with a diverse pool of research participants
- Effective verbal and written communication skills
- Ability to collaborate within multi-disciplinary team settings
- Availability to work evenings, overnight and weekends if called for under the study protocols
- Travel may be required
- Bachelor’s degree in Sciences or health-related discipline (Preferred)
