Employer Industry: Healthcare Research

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Work remotely with a stable, secure, compliant workstation
- Collaborative work environment with a focus on ethical research practices
- Engage in regional and national conferences and educational events
- Comprehensive support for research staff on submissions and compliance

What to Expect (Job Responsibilities):
- Serve as a liaison and information resource to investigators regarding federal requirements for human research
- Attend and document IRB meetings, ensuring compliance with federal regulations
- Review and confirm modifications required for IRB protocol approvals
- Compose correspondence to investigators regarding required changes for research approval
- Collaborate with research personnel to provide guidance on IRB policies and procedures

What is Required (Qualifications):
- Bachelor's degree required; Master’s or doctoral degree in a healthcare-related area strongly preferred
- At least 3 years of relevant experience in clinical research or regulatory affairs
- Knowledge of federal, state, and local laws governing human-subjects research
- Certified IRB professional (CIP) credential in good standing or must pass the certification exam within the first 90 days of employment
- Availability for Monday - Friday EST business hours

How to Stand Out (Preferred Qualifications):
- Experience in human subject protection programs
- Familiarity with the Belmont Report and Nuremberg Code
- Strong communication and interpersonal skills
- Ability to identify opportunities for process improvements
- Participation in process improvement activities

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