In House Clinical Research Associate - Single Sponsor

at  Icon plc

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.
We are currently searching for an In-House Clinical Research Associate (IHCRA) to be client dedicated to a global pharmaceutical company who have a really positive market reputation. As an In House CRA, you will perform remote visits and develop and maintain project management documents and tracking tools essential to all aspects of managing clinical studies.

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

• Working with the Project Manager and core study team to ensure that project deliverables are completed in accordance with contract and client expectations
• Remote Visits
• Facilitating project team and client meetings/teleconferences, e.g. scheduling, booking resources and preparing meeting materials, agendas and meeting minutes
• Facilitating internal and external system access for study participants
• Developing and maintaining project tracking tools and generating project status reports
• Generating and maintaining project specific documents, e.g. project specific training plan, organizational charts, contact lists, newsletters
• Managing site supplies/printed study materials and coordinating timely distribution to sites
• Coordinating project specific training setup and assignment of this to team members through internal systems
• Facilitating project team compliance, e.g. project specific training, CTMS and TMF compliance
• Assisting with TMF maintenance and ongoing Quality Control
• Assisting in the Submissions process: preparation of submission packages for IRB/ERC and support of submissions for regulatory agency

You are:

• Scientific background or equivalent experience in healthcare
• Prior experience working as a Study Coordinator (Clinical Trials), Clinical Trial Coordinator, Clinical Trial Associate/Assistant, In House CRA preferred.
• Strong IT skills, in particular MS Excel and the ability to take and type up accurate minutes
• You will be a strong communicator and have the ability to multi task and work effectively under pressure.
• Fluent English and German