ICON Plc

Senior Clinical Research Associate - Cardio Device - US Regional


PayCompetitive
LocationBlue Bell/Pennsylvania
Employment typeFull-Time

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  • Job Description

      Req#: JR136831
      Employer Industry: Clinical Research and Healthcare

      Why consider this job opportunity:
      - Opportunity for career advancement and growth within the organization
      - Competitive salary and comprehensive benefits package
      - Flexible work-from-home arrangement
      - Supportive and inclusive work environment that values diversity
      - Access to a global network of professionals for personal and family well-being support
      - Chance to contribute to innovative clinical trials in the cardiovascular/electrophysiology medical device space

      What to Expect (Job Responsibilities):
      - Oversee and manage clinical trial activities to ensure compliance with protocols and regulatory requirements
      - Act as the primary contact for assigned trial sites, facilitating communication and engagement with investigators and site staff
      - Monitor site activities, ensuring quality data collection and participant safety throughout the trial lifecycle
      - Collaborate with trial teams to develop and implement recruitment strategies and manage site study supplies
      - Maintain inspection readiness by ensuring accurate documentation and data management in trial management systems

      What is Required (Qualifications):
      - Bachelor’s Degree required, preferably in Life Science, Physical Science, Nursing, or Biological Science
      - Minimum of 5 years of monitoring experience in clinical research
      - Strong understanding of Good Clinical Practice, ICH guidelines, and local regulatory requirements
      - Proven ability to effectively communicate and collaborate within a team environment
      - Willingness to travel up to 65% for site visits and monitoring activities

      How to Stand Out (Preferred Qualifications):
      - Experience in electrophysiology or cardiac medical device monitoring
      - Analytical/risk-based monitoring experience
      - Strong organizational skills and ability to drive patient recruitment strategies
      - Familiarity with various clinical trial management systems and databases
      - Previous mentoring experience or involvement in process improvement initiatives

      #ClinicalResearch #HealthcareJobs #RemoteWork #DiversityAndInclusion #ClinicalTrials

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  • About the company

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