Employer Industry: Healthcare Research and Regulatory Affairs

Why consider this job opportunity:
- Opportunity for career advancement and growth within a leading healthcare organization
- Work remotely with flexible scheduling options
- Engage in meaningful work that supports human subject research and ethical compliance
- Participate in regional and national conferences and educational events
- Collaborative work environment with a focus on diversity and inclusion

What to Expect (Job Responsibilities):
- Serve as a liaison and information resource for investigators and research personnel regarding federal requirements and policies
- Attend and participate in IRB meetings, conducting reviews of research involving human subjects
- Compose and maintain accurate minutes of IRB meetings and ensure compliance with quorum requirements
- Review and confirm necessary modifications for human research protocols to secure IRB 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 preferred
- Minimum of 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 ability to obtain within the first 90 days of employment
- Strong organizational and communication skills

How to Stand Out (Preferred Qualifications):
- Experience in a research or regulatory affairs setting with a focus on human subjects
- Familiarity with ethical principles and concepts related to human subjects research
- Previous experience attending and documenting IRB meetings

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