Clinical Research Associate

1 week ago


Beijing, Beijing, China CDS Fortrea Inc. Full time
Transforming Drug Development with Fortrea

As a leading global contract research organization (CRO), Fortrea is dedicated to delivering innovative clinical development solutions to pharmaceutical, biotechnology, and medical device companies. Our team of experts is passionate about overcoming barriers in clinical trials and revolutionizing the development process.

Responsibilities:
  • Study startup, including site selection and recruitment of potential investigators
  • Negotiating study budgets and ensuring compliance with regulatory requirements
  • Conducting site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, and liaison with vendors
  • Site management, including SAE reporting, production of reports, and follow-up of SAEs
  • Reviewing Case Report Forms (CRFs), generating and resolving queries against established data review guidelines
  • Supporting the organization of meetings and other tasks as instructed by supervisor
Requirements:
  • University/college degree (life science preferred) or certification in a related allied health profession
  • Relevant clinical research experience in pharmaceutical or CRO industries
  • Basic understanding of ICH Guidelines and GCP, including regulatory requirements
  • Basic understanding of the clinical trial process
  • Proficient English language skills

Fortrea is committed to fostering a collaborative workspace where personal growth is nurtured, enabling our team members to make a meaningful global impact. If you are a motivated problem-solver and creative thinker who shares our passion for overcoming barriers in clinical trials, we encourage you to apply for this exciting opportunity.



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