United States

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Onsite

Job Summary

As a Clinical Research Associate (CRA) at Thermo Fisher Scientific, you will engage in impactful work that contributes positively on a global scale. Your role will involve ensuring audit readiness and forming strong collaborative partnerships with investigational sites, enhancing the efficiency and compliance of clinical research operations.

Responsibilities

  • Ensure that all activities comply with regulatory standards and sponsor requirements.
  • Facilitate and maintain effective working relationships with investigational sites.
  • Prepare for audits by organizing necessary documentation and processes.
  • Monitor the progress of clinical trials to ensure timely and accurate reporting.

Qualifications

  • Strong understanding of clinical research processes and regulations.
  • Proven ability to build relationships with study sites.
  • Excellent organizational skills and attention to detail.
  • Experience in preparing for and conducting audits.

Thermo Fisher provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
To apply for this job, please upload your resume.
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Clinical Research Associate (CRA)
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