Clinical Process Change Manager
Clinical Process Change Manager At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.
UK jobs. Bigger possibilities.
136,000+ live jobsHybrid in Livingston·Added 27 days ago (last checked 12 Oct)
Permanent contract
Per the ad.
Hybrid
Office and home days — the ad has the split.
Be near Livingston for hybrid days
No relocation package mentioned.
Cycle to work scheme
Commuter benefits named in the ad.
Nice to have
Clinical Data Coordinator II
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.
We're looking for a Clinical Data Coordinator II to join our growing team in Livingston, UK. This is a fantastic office based opportunity for recent graduates and early-career professionals who want to build hands-on experience in clinical research while working alongside experienced specialists in a collaborative, office-based environment.
At ICON plc, you'll help support the design and analysis of clinical trials, work with real-world medical data, and develop valuable skills that contribute to the development of innovative new treatments. With strong mentorship and learning opportunities, this role offers an excellent starting point for building a career in the clinical research industry.
(Mandatory start date in November 2026)
Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.
Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management.
Address data related questions and recommend potential solutions.
Identify root cause to systematically resolve data issues.
Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry.
Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).
Strong attention to detail and the ability to work effectively in a fast-paced environment.
Excellent communication skills and the ability to collaborate with cross-functional teams.
Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.
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:
Visit our careers site to
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
ICON is a clinical research organisation (CRO) providing outsourced clinical development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company describes itself as the world's leading clinical research organisation and operates at global scale, with employees in 119 locations across 53 countries.
Its services span clinical and scientific operations, decentralised clinical trials, early clinical and laboratory services, medical imaging, regulatory affairs, consulting, commercialisation, medical writing, biometrics and outcome measures. ICON works across sectors including pharmaceuticals, biotech, medical devices and government and public health, and across therapeutic areas such as oncology, cardiovascular, central nervous system, vaccines and rare and orphan diseases.
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