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Clinical Research Associate


This job is now closed

PayCompetitive
LocationRemote
Employment typeFull-Time
  • Job Description

      Req#: 7950
      Employer Industry: Pediatric Specialty Care

      Why consider this job opportunity:
      - All employees are eligible for medical coverage on their first day
      - Retirement savings plan with matching contributions of up to 6% after one year of service
      - Paid time off, life insurance, short-term and long-term disability benefits available for full-time and part-time employees
      - Opportunities for tuition reimbursement and additional benefits like pet insurance
      - Engaged in a learning environment that values innovation and critical thinking
      - Recognized as one of the best mid-sized employers by Forbes in 2025

      What to Expect (Job Responsibilities):
      - Coordinate and implement system-wide processes to standardize clinical research operations
      - Facilitate research activities through collaborative communications with sites and external entities
      - Maintain Human Subjects and Regulatory documents for submission to the centralized Institutional Review Board
      - Monitor compliance with ethical standards and regulations throughout the clinical research process
      - Provide education and training for research personnel related to clinical research activities and regulations

      What is Required (Qualifications):
      - Minimum of 3 years of clinical research experience, including site management and study management
      - Bachelor's Degree in clinical research, science, or a healthcare-related field, or 5 years of relevant experience in clinical research administration
      - Knowledge of federal regulations regarding clinical research compliance
      - Ability to interact effectively with various stakeholders, including investigators and research staff
      - Commitment to human subjects' protection and ethical practices in research

      How to Stand Out (Preferred Qualifications):
      - Experience in coordinating multi-site clinical studies
      - Job-related experience in the oversight or management of human clinical studies
      - Familiarity with clinical research genomics and sample-processing workflows
      - Certification as a Clinical Research Coordinator (CCRC) or Clinical Research Associate (CCRP)
      - Master's Degree in clinical research, science, or a healthcare-related field

      #PediatricCare #ClinicalResearch #HealthcareJobs #CareerGrowth #EthicalStandards

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      We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.
  • About the company

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