As a CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

• Clinical Trial Assistant, assists with local project management activities of clinical trials from start-up through to closeout activities. Work in close collaboration with the Global Trial leader (GTL) to ensure overall study delivery at the country level.

  • Schedules study management team meetings for each project assigned and maintains documentation from meetings.
  • Assists in management of project budgets and Affiliate spend, reconciliation of invoices, final budget and liaises with Accounts payable, as necessary.
  • Ensures study compliance by maintaining and updating trial management systems, Clinical Trial Management System (CTMS), Trial Master File (eTMF) and Trial Master Source (TMS) ensuring upto-date, complete and accurate status.
  • Maintains internal project specific study sites to ensure availability of all central project documents.
  • Liaises with external service providers and contract research organizations as needed.
  • Keeps oneself inspection ready and knowledgeable for current work by complying with relevant
    training requirements.
  • Keeps the trial in compliance with local regulatory requirements by organizing and ensuring IEC/HA approvals, if applicable.
  • Full utilization by timely and accurate time reporting.

What do you need to have?

• Bachelor’s degree or equivalent experience
• Excellent independent time management skills.
• Experience in clinical research experience in the pharmaceutical industry or CRO. At least 1 year in a CTA role.
• Fluency in English

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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