Administrative Skills, Clinical Data, Clinical Research, Communication Skills, Data Entry, Data Management, Detail Oriented, Documentation, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Informed Consent, Meeting Minutes, Pediatrics, Regulations, Training/Teaching Materials
- Assist with screening, recruitment, and enrolling of participants for research, following IRB approved protocols.
- Obtain informed consent and compliant, detailed documentation of research activities.
- Assist with research - based data abstraction, data input and management of a clinical registry database.
- Coordinate with study patients about completion of surveys, questionnaires, and scheduling bio-collections.
- Provide administrative support by preparing and maintaining regulatory documentation, preparing weekly meeting minutes, preparing educational materials, attending educational events, and other administrative duties as assigned.
- Assist with providing oversight and program support to student interns and student workers.
Knowledge, Skills & Abilities:
- Detail orientated.
- Demonstrated ability to work autonomously.
- Ability to handle confidential and sensitive information.
- Ability to communicate effectively with different groups/individuals.