Clinical Data Science Lead (All Levels)

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.

With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

The Role

We are currently seeking a Clinical Data Science Lead to join our diverse and dynamic team. As a Clinical Data Science Lead at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

• Lead and oversee the development and implementation of data analysis strategies for clinical trials.
• Ensure clinical data management review requirements are put into production per the study’s protocol risk evaluation and integrated data review plan (IDRP), and that ongoing data review activities are compliant with study plan requirements.
• Centrally review clinical data at aggregate level, using analytic reporting tool(s) to support the identification of risks and data patterns/trends. Mitigate risks by using signal detection and quality indicators.
• Drive innovation in data science techniques to enhance the efficiency and accuracy of clinical trial processes.
• Provide leadership and mentorship to a team of data scientists and coordinators, fostering a culture of continuous learning and development.

Your profile

• Bachelor’s degree in quantitative, scientific or health related field required.*
• 5 years of relevant experience required.
• In-depth knowledge of the drug development process including risk-based monitoring principles, clinical and biometrics procedures, workflows, and software systems.
• Excellent skill in aggregate data review and interpretation using visualization/ analysis software, e.g., JReview, Tableau, SAS
• Excellent project management and leadership skills
• Advanced ability to proactively represent data management internally and externally for all study related items and find pragmatic solutions in compliance with regulatory requirements and policies.

* Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above. All employees must read, write and speak fluent English and host country language.

Benefits of Working in ICON
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

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, 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.

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