• Job Description

  Req#: RQ4054605
  Employer Industry: Healthcare Research and Regulatory Affairs
  
  Why consider this job opportunity:
  - Salary up to $102,596.00 annually
  - Full-time remote role with flexibility to work from most US states
  - Opportunity for career advancement and professional growth within the organization
  - Comprehensive benefits package and recognition programs to celebrate contributions
  - Engage in meaningful work that supports human subject protection in research
  - Participate in regional and national conferences and educational events
  
  What to Expect (Job Responsibilities):
  - Serve as a liaison and information resource to investigators and research personnel on federal requirements and policies for human research approval
  - Attend IRB meetings to conduct initial and continuing reviews of research activities involving human subjects
  - Ensure quorum requirements are met for protocol reviews at convened meetings
  - Compose detailed minutes of IRB meetings, documenting attendance, actions taken, and voting outcomes
  - Review human research protocol submissions to ensure compliance with applicable regulations and institutional policies
  
  What is Required (Qualifications):
  - Bachelor’s degree required; Master’s degree strongly preferred
  - Certified IRB professional (CIP) credential in good standing or must pass certification exam within the first 90 days of employment
  - At least 3-5 years of related research or regulatory affairs experience
  - Knowledge of federal, state, and local laws and regulations governing human-subjects research
  - Familiarity with ethical principles and concepts for the responsible conduct of human subjects research
  
  How to Stand Out (Preferred Qualifications):
  - Experience working with federal and state regulatory agencies related to human subjects research
  - Proven ability to communicate effectively with diverse stakeholders in a research environment
  - Participation in process improvement activities within an IRB or similar setting
  - Experience in composing detailed meeting documentation and correspondence
  - Engagement in ongoing professional development related to IRB practices and regulations
  
  #HealthcareResearch #RegulatoryAffairs #RemoteWork #CareerAdvancement #IRBCompliance
  
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• About the company

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