University of Arkansas

Regulatory Specialist II


PayCompetitive
LocationLittle Rock/Arkansas
Employment typeFull-Time

This job is now closed

  • Job Description

      Req#: R0079304
      Employer Industry: Healthcare Research and Clinical Trials

      Why consider this job opportunity:
      - Competitive salary commensurate with education and experience
      - Comprehensive benefits package, including medical, dental, and vision plans
      - Up to 10% matched contribution for retirement savings
      - Education discounts for staff and dependents
      - Opportunities for career training and professional development
      - Supportive and collaborative work environment focused on improving patient care

      What to Expect (Job Responsibilities):
      - Ensure regulatory compliance and administrative management for multiple clinical trials
      - Collaborate with investigators, industry sponsors, and contract research organizations
      - Organize complex projects while maintaining attention to detail and effective communication
      - Apply knowledge of local policies and federal regulations in support of clinical trial objectives
      - Contribute to cross-functional teams to ensure effective workflow and adherence to quality standards

      What is Required (Qualifications):
      - Bachelor’s degree plus 3 years of experience in clinical research related to FDA Regulatory Affairs, or
      - High School diploma, GED, or formal education equivalent plus 7 years of research experience in lieu of a bachelor’s degree
      - Minimum of 3 years of clinical research experience with proficiency in study planning, regulatory start-up, and maintenance
      - Ability to obtain CRS certification within 2 years of hire
      - Must possess proof of legal authority to work in the United States on the first day of employment

      How to Stand Out (Preferred Qualifications):
      - Experience working with pharmaceutical company sponsors and research staff
      - Familiarity with the Code of Federal Regulations and human research conduct guidelines
      - Strong organizational skills and ability to manage multiple projects simultaneously
      - Effective problem-solving skills and ability to work in a fast-paced environment
      - Excellent verbal and written communication skills

      #HealthcareResearch #ClinicalTrials #RegulatoryAffairs #CareerOpportunity #HealthcareCareers

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  • About the company

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