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Clinical Research Associate

2 months ago

Swansea, City and County of Swansea, United Kingdom ICON Full time
Role:

Clinical Research Associate

As a Clinical Research Associate at ICON, you will be part of a global team dedicated to delivering high-quality clinical research services to our clients. Your primary responsibility will be to manage investigator sites and monitor activities for assigned clinical studies throughout the trial lifecycle.

Key Responsibilities:

  • Full ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance with the clinical monitoring plan.
  • Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.
  • Conducting monitoring visits and ensuring compliance with ICH-GCP guidelines and local and international regulatory requirements.
  • Collaborating with cross-functional teams to ensure seamless execution of clinical trials.

Requirements:

  • Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.
  • A working knowledge of ICH-GCP guidelines and local and international regulatory requirements.
  • Education to degree level in a life science discipline or be a licensed healthcare professional.

What We Offer:

At ICON, we are committed to developing our employees in a continuous learning culture. We offer a comprehensive and competitive total reward package that comprises an excellent level of base pay, variable pay, and recognition programs. Our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to support you and your family at all stages of your career.