IHCRA

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

Working fully embedded within one of our pharmaceutical clients the Clinical Trial Assistant will develops/maintains study documents and utilizes company systems to manage clinical biomedical studies. Provides administrative support to project team members in clinical operations and project management. Works with the project team to ensure that projects are completed in accordance with contract and client expectations. Completes project management tasks as assigned by the study project manager/project director. Project management tasks will provide opportunities to broaden exposure to project management activities and to develop core project management skills.

Responsibilities:

• Organizes project team and client meetings including scheduling, creating meeting materials, binders, agendas and meeting minutes, etc.
• Assumes project management tasks as assigned by the study project manager/project director with final approval of deliverables completed by the study project manager/project director.
• Organizes study information and supplies. Generates and maintains organizational charts, team calendar, newsletters, mass mailings, project specific information including but not limited to: process flow charts, contact lists, holiday lists, study website, mailing labels. Tracks, dispatches and maintains study supplies following applicable company processes.
• Manages internal and client project reporting. Generates and reviews for accuracy reports to facilitate project status and financial reporting. Completes system updates and queries.
• Supports project manager with financial tasks. Has oversight of purchase order process including creating and processing purchase orders and processing study invoices. May process Investigator payments.
• May support preparation of study files by maintaining and distributing project documents. Ensures documents within the electronic trial master file comply with filing/naming guidelines and have the correct status.

• Uses the learning management system to assign project specific training to team members and tracks training compliance.

You are:

Passionate and responsible.

Here at ICON we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

• BA/BS or equivalent or any relevant and qualifying training with a minimum of 1/2 years of relevant clinical trial experience
• Expert knowledge of applicable systems/processes
• Proficiency in using applicable business applications including word processing, spreadsheet, presentation programs
• Ability to use basic principles of timeline management, project financials, and risk management
• Robust knowledge of the company’s industry and service offerings
• Working knowledge of relevant regulations
• Working knowledge of drug/patient safety procedures and regulations
• Familiarity with medical terminology
• Read, write and speak fluent in English and Italian.
• General knowledge of risk management
• Advanced knowledge of several functional activities, use of functional specific processes or systems, and/or therapeutic knowledge based on previous work assignments
• Understanding of basic roles within the clinical research organization including but not limited to clinical operations, biometrics, regulatory and drug safety.
• Understanding of project financial management including forecasting and change order development
• Ability to use logic to effectively to complete assigned project management tasks
• Ability to serve as a back up to the project manager in a limited capacity based upon assigned project management tasks.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

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

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 or submit a request here.

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.