Clinical Trial Manager

As a Clinical Trial Manager based in the Netherlands, (Eindhoven area) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

Drive adoption of compliant clinical study execution practices throughout active in clinical studies including research and testing of products involving human beings • Develop and maintain the policies and procedures for the Clinical Operations function of Clinical and Medical Affairs. • Support, update and maintain the Clinical Trial Management System application for clinical study execution and reporting.

The Clinical Operations Manager supports product development and in-market success through clinical evidence creation that speaks to fundamental value propositions. • Provide leadership in execution and management of clinical studies to deliver high quality data to support client’s businesses on time, within budget and in compliance to all applicable regulations and clients’ procedures • Support output to Daily Leadership Board via maintenance of the Clinical Trial Management System. • Ensure projects supported by clinical operations team have been prioritized, budgeted, and resourced by Product Managers. • Ensure communication with team is strong, ensuring feedback is provided in real time through provision of mentoring and leadership coaching. • Ensure global process and procedures for clinical study execution are followed and gaps in understanding addressed through regular training. • Ensure all audit requests, responses, and effectiveness checks are supported, addressed, and closed according to jointly agreed timelines

BS/BA in scientific or relevant discipline. • BS/BA in scientific or relevant discipline. • BS/BA or Advanced Degree in Health Sciences related field. Experience & Background Self-motivated individual who is able to manage multiple tasks and priorities in an efficient manner. • Must be able to communicate effectively across a diverse global network of businesses and be comfortable in a virtual environment. • Minimum of 5+ years of combined CRA or Clinical Study Management experience in a pharmaceutical, medical device or biologic clinical studies research setting. • Site assessment/monitoring g experience is required. • Effective organizational, communication, and project team skills. • Demonstrated expertise of GCP, ISO and FDA regulatory requirements for the conduct of research involving human subjects is required. Must be proficient at Self-motivated individual who is able to manage multiple tasks and priorities in an efficient manner. • Must be able to communicate effectively across a diverse global network of businesses and be comfortable in a virtual environment. • Minimum of 7+ years of combined CRA or Clinical Study Management experience in a pharmaceutical, medical device or biologic clinical studies research setting. • Site assessment/monitoring experience is required. • Effective organizational, communication, and project team skills. • Demonstrated expertise of GCP, ISO and FDA regulatory requirements for the conduct of research involving human subjects is required.

Fluently in Dutch and English.

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

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, 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 through the form below.

https://careers.iconplc.com/reasonable-accommodations

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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