Clinical Research Associate

4 weeks ago

Belfast, United Kingdom Pharmiweb Full time
Job Summary

We are seeking a highly skilled Clinical Research Associate to join our team in the pharmaceutical industry. As a Clinical Research Associate, you will be responsible for coordinating and conducting clinical trials, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to deliver high-quality results.

Key Responsibilities
  • Coordinate and conduct clinical trials, including site initiation, monitoring, and close-out visits
  • Ensure compliance with regulatory requirements, including ICH, GCP, and local regulations
  • Collaborate with cross-functional teams, including project managers, investigators, and sponsors
  • Develop and maintain strong relationships with investigators and sites
  • Ensure timely and accurate data collection and reporting
  • Participate in feasibility studies and site selection
  • Conduct regular monitoring visits and ensure compliance with SOPs
  • Maintain accurate and complete records of all trial-related activities
  • Participate in training and mentoring new staff
Requirements
  • 2+ years of independent CRA experience in a pharma or CRO environment
  • Sciences degree
  • Experience in oncology, haematology, rare diseases, or vaccines
What We Offer

We offer a competitive salary, annual leave entitlements, health insurance, retirement planning, and a range of other benefits to support your well-being and work-life balance. Our diverse culture rewards high performance and nurtures talent, and we are committed to providing an inclusive and accessible environment for all candidates.

At ICON, diversity, inclusion, and belonging are fundamental to our culture and values. We are proud of our diverse workforce and the work we've done to become a more inclusive organisation. We are dedicated to providing an inclusive and accessible environment for all candidates and employees.

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