Clinical Trial Assistant

ICON; Arezzo; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

ICON is hiring a Clinical Trial Assistant to support our pharmaceutical clients. This role involves managing trial documentation and coordinating study activities, offering a chance to contribute to drug development. Successful candidates will exhibit strong organizational skills, adaptability, and proficiency in English.

Servizi

Comprehensive total reward package

Best-in-class employee benefits

Supportive wellbeing initiatives

Competenze

• Experience as a CTA or Study Coordinator in the pharmaceutical industry.
• Ability to work in a dynamic environment and prioritize tasks.
• Professional proficiency in English.

Mansioni

• Manage Trial Master File (TMF) creation and ensure document compliance.
• Coordinate local data entry and maintain study management systems.
• Prepare and review site communication documents.

Conoscenze

Organization

Communication

IT skills

Descrizione del lavoro

As a Clinical Trial Assistant , you will be dedicated to one of our global pharmaceutical clients; with whom ICON shares a culture of innovation, flexibility, and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in our exclusive programs.

The Clinical Trial Assistant assists in the coordination and administration of the study activities from the start-up to execution and close out, and within the Study Team to ensure quality and consistency of interventional study deliverables to time, cost, and quality objectives. As a Clinical Trial Assistant, you will have the opportunity to experience the full lifecycle of a project and genuinely contribute to drug development and improving patients’ lives.

What you will be doing :

• Trial Master File (TMF) creation and management
• Co-ordinate entry and maintain local data into study management systems including setting up new studies
• Ensure collection, review, track and provision of appropriate clinical documents to support regulatory submission
• Track and maintain adequate study-related supplies in the office and facilitate their distribution to sites, including preparing and distributing Study File Binders and Site Initiation presentations / materials
• Process, reconcile, distribute and track essential documents and submit them to local archive in compliance with SOPs
• Complete tracking documentation as applicable including but not limited to spreadsheets, study and contract tracker
• Prepare and review site communication documents
• Set-up / maintain courier accounts and organize shipments

You are :

Experience as a CTA, within the pharmaceutical industry or CRO or as Study Coordinator and Data Manager

Excellent organization skills

Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business

Strong IT skills

Strong communication with the ability to multitask and work effectively under pressure

Professional proficiency in English

Why ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, 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 - both now, and into the future.

Our success depends on the knowledge, capabilities, and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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.

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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