At a Glance
- Tasks: Lead clinical data management strategies and collaborate with teams for impactful research.
- Company: Join ICON plc, a top-tier healthcare intelligence and clinical research organisation.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
- Other info: Diverse culture with excellent career growth and travel opportunities.
- Why this job: Make a difference in clinical trials while working with cutting-edge data science techniques.
- Qualifications: Bachelor's degree and 8-10 years in clinical data management required.
The predicted salary is between 55000 - 65000 £ per year.
Overview Clinical Data Manager, Sponsor Dedicated.
ICON plc is a world-leading healthcare intelligence and clinical research organization.
We’re proud to foster an inclusive environment driving innovation and excellence.
Senior CDSL (Sponsor Dedicated) – UK or France What You Will Do You will oversee clinical data science workstreams, ensuring deliverables meet quality and timeline expectations.
Key Responsibilities Leading the development and implementation of clinical data management strategies to optimize data collection, analysis, and reporting.
Collaborating with cross-functional teams to ensure the accurate integration of data science techniques into clinical trial designs.
Overseeing the analysis of clinical data to provide actionable insights that inform study decisions and outcomes.
Providing strategic guidance on data governance, quality control, and compliance with regulatory requirements.
Establishing partnerships with key stakeholders to leverage the latest advancements in data science and technology in clinical research.
Required Qualifications and Experience Bachelor's degree in Life Sciences, Computer Science, or a related field. 8 to 10 years of clinical data management experience, including Early Development and Phase I studies.
Experience leading at least three study start ups and three database locks.
Strong knowledge of clinical data management, data review, and data quality processes.
Experience participating in User Acceptance Testing and reviewing data reports.
Comfortable managing frequent real time data extracts and supporting rapid study decisions.
Experience leading post production changes and change control activities.
Experience overseeing Clinical Data Coordinators and delegated activities.
Experience managing external data vendors and third party data deliverables.
Exposure to dose escalation studies and meetings preferred.
Strong leadership skills with experience working across cross functional teams.
Proficient in data analysis tools, statistical software, and data visualization.
Excellent communication, stakeholder management, and problem solving skills.
Proactive approach with the confidence to research, resolve issues, and drive outcomes.
CRO oversight experience preferred but not required.
Willingness to travel up to 15 percent as required.
What ICON can offer you Our success depends on the quality of our people.
We’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to a competitive salary, ICON offers a range of benefits designed to support well-being and work-life balance, tailored to each country.
Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings Global Employee Assistance Programme offering 24-hour access to a global network of professionals Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, gym discounts, subsidized travel passes, health assessments, among others ICON is committed to an inclusive and accessible environment for all candidates.
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 you need a reasonable accommodation for any part of the application process, please let us know.
Interested in the role?
Apply through the standard ICON careers process. #J-18808-Ljbffr
