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.
As a Clinical Data Science Lead at ICON, you will drive data science initiatives within clinical trials, ensuring that our analyses provide meaningful insights that inform strategic decisions.
Key Responsibilities
- Serve in a support‐level capacity on a Clinical Data Management team to provide efficient and quality clinical data management products. Support the design, specifications, and development of eCRFs, ensuring adherence to company standards.
- Coordinate the development and testing of clinical data management systems edit checks and listings/reports/tools for data review
- and discrepancy management activities.
- Support the development of Data Management Plan documents that will ensure delivery of accurate, timely, consistent, and high‐quality clinical data. Works with Third Party /External data Vendors to complete the set‐up of data import and reconciliation processes.
- Perform comprehensive review of all data generated from the clinical study including Third Party/External data, SAE data and local lab data, as applicable. Oversees quality control procedures. Develop and maintain strong communications and working relationships with CDM team.
- Effectively manage project timelines and quality.
- Provide reports, status updates, feedback, and advice to key study stakeholders on the progress of data cleaning and risk identification/mitigation activities.
- Ensure CDM activities are performed in compliance with Good Clinical Practice, ICH Guidelines.
- Apply appropriate best practices and independently offer project solutions to the study team.
- Support the filing of eTMF documentation to ensure that an inspection ready environment is maintained throughout the study lifecycle.
- Provide back up support for Principal Clinical Data Lead as required.
Your Profile
- 4+ years of Clinical Data Management experience
- Ability to work under pressure demonstrating agility through effective and innovative team leadership
- Robust experience with EDC (E.g. Medidata Rave) and use of Data Review tools such as elluminate, J‐Review or Business Objects required
- Experience in Phase I/II
- Neurology experience would be desirable.
- Extensive experience in Study startup.
- Strong technical skills, including experience working with using Microsoft Excel functionality
- Fluent English (oral and written)
- Strong understanding of drug development and biopharmaceutical industry required.
- High attention to detail including proven ability to manage multiple, competing priorities
- Excellent written and oral communication skills
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 maximize savings and plan with confidence for the years ahead.
- 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.
- Life assurance
- 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 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
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 to apply