ICON Plc

Clinical Research Associate - Central/East Coast


PayCompetitive
LocationBlue Bell/Pennsylvania
Employment typeFull-Time

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  • Job Description

      Req#: JR135897
      Employer Industry: Clinical Research Organization

      Why consider this job opportunity:
      - Competitive salary and various annual leave entitlements
      - Comprehensive health insurance offerings to suit you and your family’s needs
      - Competitive retirement planning options to maximize savings for the future
      - Global Employee Assistance Programme providing 24-hour access to a network of specialized professionals for well-being support
      - Opportunities for professional development and progression within a diverse and inclusive work environment
      - Ability to work independently while contributing to innovative clinical trials

      What to Expect (Job Responsibilities):
      - Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
      - Ensure protocol compliance, data integrity, and patient safety throughout the trial process
      - Collaborate with investigators and site staff to facilitate smooth study conduct
      - Perform data review and resolve queries to maintain high-quality clinical data
      - Contribute to the preparation and review of study documentation, including protocols and clinical study reports

      What is Required (Qualifications):
      - Bachelor's degree in a scientific or healthcare-related field
      - Minimum of 12 months of onsite monitoring experience as a Clinical Research Associate
      - In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
      - Strong organizational and communication skills, with attention to detail
      - Ability to travel at least 60% of the time and possess a valid driver’s license

      How to Stand Out (Preferred Qualifications):
      - Experience as a Clinical Research Associate I, II, or Senior CRA
      - Familiarity with advanced data analysis techniques
      - Proven ability to work in a fast-paced environment and handle multiple projects simultaneously
      - Previous experience in a global clinical trial setting
      - Knowledge of additional languages is a plus

      #ClinicalResearch #HealthcareCareers #CareerOpportunity #EmployeeBenefits #DiversityAndInclusion

      We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
      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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