Associate Director Data Analyst
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Job overview
The Associate Director Data Analyst supports the design of clinical programs and trials by combining internal and external data, analyses, and insights. The role informs clinical trial design, planning, and execution, including trial placement and patient accessibility. It also contributes to integrated datasets, analytic capabilities, standardization across therapeutic areas, and the evaluation of real-world data assets.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Associate Director, Data Analyst
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
The purpose of the Associate Director Analysis role is to support the design of clinical programs and trials by bringing together internal and external data and information (e.g. contemporary information on standard of care across the globe, understanding of patient pathways that can make trials more accessible within those geographies, interpretation of disease prevalence, etc.), analyses and insights to drive excellence in clinical trial design, enabling more efficient planning and execution to speed medicines to patients.
What You Will Do:
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Analyze, create visualizations in support of, and communicate data, insights, and recommendations from information in various internal and external sources to support processes around the placement of clinical trials and other key analysis that could span CDDA leaders, functions, and teams.
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Create and adapt queries to extract vital data from internal and external data sources for prompt analysis on clinical design questions
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Extract and curate data from multiple data sources to build integrated datasets and visualizations that will drive recommendations and decisions
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Partner cross-functionally to ensure consistency, completeness and robustness in data feeding into core analytic capabilities
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Apply novel techniques to add efficiency and automation into Clinical Trial Design and CDDA capabilities
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Responsible for driving standardization in design within and across therapeutic areas via development and management of taxonomies
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Lead the evaluation and use of real-world data assets to inform design
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Manage data source vendor relationships and contracts alongside with procurement
Your Profile:
Required qualifications and experience:
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Bachelor’s Degree in a scientific, analytic, or health-related field
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3 - 5 years experience in drug development or science-related field
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:
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Various annual leave entitlements
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A range of health insurance offerings to suit you and your family’s needs.
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Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
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Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
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Life assurance
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Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. 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 or submit a request here (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.
Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply
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