As a Clinical Quality Compliance Lead you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing: Job Summary Under the leadership of the Operations Quality Lead, supports or may lead inspection readiness initiatives Creates process and tools to achieve inspection readiness within Development Operations With DOQ leadership, helps to facilitate the growth of opportunities for collaboration with QA, collaborating with the Operations Quality Lead and the Operations Quality Manager General Responsibilities Develop and maintain guidance and process to facilitate DOQ support of Study Teams Under the leadership of the Operations Quality Lead, develop, contribute, and support facilitation, presentation, and communication of GCP Lessons Learned, GCP Cases, or other trending analysis Provide training or awareness for new or established processes or guidance provided by DOQ Collaborate in developing and presenting DOQ content for distribution within the organization Author relevant content for the DOQ SharePoint site Act as lead on specified DOQ workstreams or assigned DOQ initiatives In collaboration with the Operations Quality Lead and the Operations Quality Manager, provide consultation and support for ad hoc requests that are sent to DOQ Consult, develop, or identify opportunities for continuous improvement projects Develop, review, and analyze KQI or metrics that may identify emergent issues or trends or demonstrate strong adherence to quality within Development Operations Stay current with knowledge of clinical trial requirements, ICH GCP guidelines, and global regulatory requirements for the management of clinical trials Facilitate and support cross-functional stakeholder engagement to ensure adequate representation for consultation towards consensus Develop matrix relationships to involve process experts and conduct improvement activities Collaborate with DOQ Leadership to ensure integration, alignment, and consistent messaging across the organization Promote a culture of quality, continuous improvement, and operational excellence that engages colleagues in positive dialogue consulting and supporting in all we do You are: Bachelor's degree or equivalent with a strong emphasis on science or quality management Minimum of 5 years' experience in a pharmaceutical, bio-pharmaceutical, or Contract Research Organization company, or equivalent Minimum of 3 years' experience in quality role Must have working knowledge of ICH GCP and other relevant regulatory/health authority experience Ability to travel 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.