Human Research Protection Program Analyst
New
B
Banner HealthClinical Research
The preferred candidate must live local to our facility; 901 E Willetta St, Phoenix, AZ 85006, Sunday-Saturday, 8AM-5PMPart-TimeMiddle
Salary not disclosed
Apply NowOpens the employer's application page
Job Details
- Experience
- At least two years of relevant work experience
- Required Skills
- ComplianceHIPAA
Requirements
- Bachelor’s degree in clinical research, compliance, or a health-related field.
- At least two years of relevant work experience.
- Strong understanding of regulatory affairs, IRB management, or clinical research operations.
- Experience working with an HRPP, IRB, or in research regulatory affairs.
- Familiarity with HIPAA research regulations, ethical principles, and IRB policies.
- Excellent organizational and task management skills.
- Ability to effectively communicate with physicians and research stakeholders.
- Proficiency in using electronic research submission systems.
- Ability to multitask and prioritize in a fast-paced environment.
Responsibilities
- Process RDC and IRB submissions and complete pre-reviews of research protocols.
- Prepare meeting agendas and minutes for full IRB/RDC review processes.
- Manage studies and the submission process within the iRIS electronic system.
- Provide in-person and phone consultation to research staff regarding IRB and RDC application preparations.
- Coordinate the orientation, education, and training of board members and research staff.
- Develop and update IRB/RDC SOPs, guidance documents, and policy procedures.
- Monitor compliance with annual reporting requirements and maintain centralized tracking systems.
View Full Description & ApplyYou'll be redirected to the employer's site
