At a Glance
- Tasks: Support clinical trials by managing data and collaborating with experienced specialists.
- Company: Join ICON plc, a leading healthcare intelligence and clinical research organisation.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
- Other info: Inclusive culture focused on innovation and personal growth.
- Why this job: Kickstart your career in clinical research with hands-on experience and mentorship.
- Qualifications: Bachelor's degree in Life Sciences or Healthcare; knowledge of clinical data management preferred.
The predicted salary is between 30000 - 40000 £ per year.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We’re looking for a Clinical Data Coordinator II to join our growing team in Livingston, UK. This is a fantastic 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.
What You Will Be Doing
- 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.
- Track and communicate 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.
Your profile
- 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
- 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 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.
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.
Clinical Data Coordinator II in Livingston employer: ICON Strategic Solutions
At ICON plc, we pride ourselves on being a world-leading healthcare intelligence and clinical research organisation that values innovation and inclusivity. Located in Livingston, UK, our office-based environment offers recent graduates and early-career professionals the chance to gain hands-on experience in clinical research while benefiting from strong mentorship and a culture that prioritises employee growth and well-being. With competitive salaries and a comprehensive range of benefits designed to support work-life balance, ICON is an excellent employer for those looking to make a meaningful impact in the clinical development field.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Data Coordinator II in Livingston
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. A friendly chat can open doors and give you insights that job descriptions just can't.
✨Tip Number 2
Prepare for interviews by practising common questions related to clinical data management. We recommend role-playing with a friend or using online resources to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your skills! Create a portfolio or a presentation that highlights your relevant projects or experiences. This can really set you apart from other candidates when you’re in front of hiring managers.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at ICON.
We think you need these skills to ace Clinical Data Coordinator II in Livingston
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Data Coordinator II role. Highlight relevant experience, especially in clinical data management and any familiarity with software like Medidata or Oracle RDC. We want to see how your background fits with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your skills align with our mission at ICON. Keep it concise but engaging – we love a good story!
Show Off Your Attention to Detail:In this role, attention to detail is key. When you submit your application, double-check for any typos or errors. A polished application shows us that you take pride in your work and are ready for the fast-paced environment we offer.
Apply Through Our Website:We encourage you to apply directly through our careers site. It’s the best way to ensure your application gets into the right hands. Plus, you can explore more about what we offer and get a feel for our culture!
How to prepare for a job interview at ICON Strategic Solutions
✨Know Your Data Management Basics
Make sure you brush up on your knowledge of clinical data management, especially if you've got experience with software like Medidata or Oracle RDC. Being able to discuss how these tools work and their importance in clinical trials will show that you're ready to hit the ground running.
✨Show Off Your Attention to Detail
In a role like Clinical Data Coordinator II, attention to detail is key. Prepare examples from your past experiences where your meticulous nature helped solve a problem or improve a process. This will demonstrate your capability to manage data accurately and efficiently.
✨Communicate Clearly and Confidently
Since you'll be collaborating with cross-functional teams, practice articulating your thoughts clearly. Think about how you can explain complex data issues in simple terms. This will not only help you in the interview but also in your future role.
✨Understand Regulatory Guidelines
Familiarise yourself with ICH-GCP guidelines and other relevant regulations. Being able to discuss these during your interview will show that you understand the compliance side of clinical research, which is crucial for the role.
