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Jobs at Parexel

Are you ready to make your mark in the healthcare industry by taking your work seriously, demonstrating empathy, and acting With Heart®? When our values align, there's no limit to what we can achieve. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top-selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. We're not just the people with expertise, we're the people With Heart®.

Clinical Trial Associate - FSP

Job ID 77743BR United Kingdom - Any Region - Home Based
We have an open position for a Clinical Trial Associate (CTA) homebased in any East/West Europe location.
Parexel FSP will offer you great pay and benefits and world class technology and training catered to your individual experience.

If impact, flexibility, and career development appeal to you, Parexel could be your next home.

Clinical Trial Associates work closely with the Project Leader and Functional Leads on project
management tasks during the entire project life cycle, contributing to achievement of study deliverables.

Main responsibilities include:
  • Serve as liaison for Project Leader, Clinical Operations Leader and Data Operations Leader and team members.
  • Support organization of meetings including meeting materials, presentations, binders, invitations, travel, and room arrangements. Track and confirm investigator meeting attendees, distribute information about meetings to the study team.
  • Request project resources and control resource utilization.
  • Arrange and assist telephone conferences, client meetings, investigator meetings as appropriate.
  • Ensure an up-to-date team list is available in the central document repository including tracking of absences and vacation lists in the central document repository, if required.
  • Compose professional business correspondence on behalf of the Project Leader/ Clinical Operations Leader and Data Operations Leader. Print, copy, and fax and/or mail correspondence, reports, documents, etc.).
  • Assist in maintaining applicable systems according to data entry guidelines.
  • Assist team members with collecting and preparation of study specific documentation, customization of forms, add version-control as well as filing in the Electronic Documents Management System.
  • Request Study related supplies and arrange distribution.
  • Control team workload in the project.
  • Control of pass-through costs invoices.
  • Complete routine administrative tasks in a timely and professional manner.

Qualifications

  • BS/BA or equivalent experience preferred.
  • A minimum of 2-3 years clinical trial experience in a similar role, preferably within the pharmaceutical or biotechnology industry.
  • Experience of working with global or European studies preferred.
  • Basic knowledge and understanding of Essential Documents, CFR and GCP/ICH
  • Proficiency with technological systems (Microsoft Office, TMF, CTMS, EDC, ECMS, Zoom)
  • Fundamental understanding of filing systems and organizational tools.

About Parexel FSP:

For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is the CRO trusted by life sciences companies to innovate keeping patients at the center of everything we do, and where an inclusive global community helps you be your best, transforming any career into a life-changing achievement.

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