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Clinical Trial Associate - FSP

Parexel International Corporation

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. QualificationsBS/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.

Job posted: 2021-11-26

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