At a Glance
- Tasks: Lead clinical data management activities and oversee data science workstreams for impactful clinical trials.
- Company: Join ICON, the world's largest FSP organisation, dedicated to improving patient outcomes.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and a supportive work-life balance.
- Other info: Be part of a diverse culture that values talent and offers excellent career growth opportunities.
- Why this job: Make a real difference in healthcare by contributing to innovative treatments and therapies.
- Qualifications: 5+ years in clinical data management with strong project management and communication skills.
The predicted salary is between 54000 - 66000 £ per year.
Senior Clinical Data Science Lead
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.
- Senior Clinical Data Science Lead - Sponsor Dedicated
- UK or South Africa
As a Senior Clinical Data Science Lead at ICON, you will lead the analysis, interpretation, and management of clinical data to drive the success of our clinical trials.
You will oversee clinical data science workstreams, ensuring deliverables meet quality and timeline expectations.
What You Will Be Doing
- Leading Clinical Data Management activities across assigned studies, from study start-up through to database closure and clean database declaration.
- Providing oversight and guidance to Data Management staff assigned to specific protocols, including mentoring and training less experienced colleagues.
- Acting as an experienced Clinical Data Management resource for global, cross-functional study teams and serving as an escalation point for study-related data management matters.
- Developing and maintaining study-specific data management components and specifications, including e CRFs, study metadata, edit checks, Data Validation Documents and protocol deviation documentation .
- Collaborating with EDC developers on the specification and design of e CRFs and database structures and contributing to EDC User Acceptance Testing (UAT).
- Managing data cleaning activities, including identifying and issuing queries, incorporating query responses, tracking query status and performing consistency checks on external data.
- Coordinating SAS programming requirements for edit checks and derivations and contributing to the preparation of data monitoring activities.
- Preparing data listings and extracts to support medical reviews, study reporting and other cross-functional activities.
- Developing and coordinating database closure plans and ensuring database closure activities are effectively communicated and delivered across the study team.
- Identifying and communicating issues that could impact study timelines or data quality and working collaboratively with study teams to address them.
- Ensuring Clinical Data Management activities are appropriately documented throughout the lifecycle of the study.
- Supporting training and education initiatives for Data Management colleagues to promote quality, productivity and consistent working practices.
Your Profile
- Bachelor’s degree or equivalent in
Natural Sciences, Informatics, Medical Documentation , or a related discipline.
5+ years of experience as a Clinical Data Manager , with significant responsibility within clinical projects and study teams.
- Strong understanding of the drug development process and extensive experience with clinical data management methodologies and technologies.
- Proven experience managing clinical data from study start-up through to clean database declaration .
- Experience working within global, cross-functional teams and collaborating with functions such as
Study Management, Medical, EDC Development, Statistics and Medical Writing .
- Demonstrated ability to interpret
Clinical Study Protocols, Statistical Analysis Plans and Medical Review Plans and translate these into appropriate data management specifications.
- Experience developing specifications including
CRFs, metadata, protocol deviation documents and edit check specifications .
- Good understanding of relevant clinical research regulations and guidelines, including
ICH and GCP .
- Experience training and/or mentoring junior Data Management colleagues, with the ability to provide guidance and act as an escalation point.
- Strong project management, organisational and self-management skills, with the ability to work independently and effectively manage priorities.
- Experience working within and helping lead global, cross-functional teams towards key study milestones such as
First Patient First Visit readiness and timely clean database declaration .
- Strong written and verbal communication skills in English, with fluent spoken English required, alongside strong local-language communication skills.
- Good understanding of IT processes and databases used within Clinical Development.
- A proactive approach to continuous learning and professional development.
- #LI-JC3
- #LI-Remote
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, Life Works, 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
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Senior Clinical Data Science Lead in Reading employer: KCR Placement
At ICON plc, we pride ourselves on being a world-leading healthcare intelligence and clinical research organisation that champions innovation and excellence. Our inclusive work culture not only fosters collaboration and mentorship but also prioritises employee well-being through competitive benefits and growth opportunities. Join us in shaping the future of clinical development while enjoying a supportive environment that values your contributions and promotes work-life balance.
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We think this is how you could land Senior Clinical Data Science Lead in Reading
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We think you need these skills to ace Senior Clinical Data Science Lead in Reading
Some tips for your application 🫡
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Tailor Your Documents to the Job:Don't use a one-size-fits-all approach! Make sure your CV and cover letter are specifically tailored for this role. Highlight any certifications you have relevant to health administration, and ensure you clearly connect your previous roles to the skills needed for the full-time position at KCR Placement. This way, you're showing them you’ve done your homework and are genuinely interested in being a part of their team.
How to prepare for a job interview at KCR Placement
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As a full-time candidate, employers will want to know how your long-term career goals align with their mission. Take some time to research KCR Placement’s values and be ready to tie your passion for health sciences administration into their objectives. Demonstrating enthusiasm and career alignment can be a game-changer in this competitive field!
