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For Companies At a Glance
- Tasks: Design and analyse clinical trials, interpreting complex medical data.
- Company: ICON plc is a leading healthcare intelligence and clinical research organisation.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
- Why this job: Join a diverse team shaping the future of clinical development with innovative treatments.
- Qualifications: Bachelor's degree in relevant field; experience in clinical data management required.
- Other info: Inclusive culture prioritising diversity and equal opportunity for all applicants.
The predicted salary is between 43200 - 72000 £ 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 are currently seeking a Principal Clinical Data Standards Consultant to join our diverse and dynamic team.
As a Clinical Data Standards Consultant at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What you will be doing
- Developing tools to aid in the implementation and compliance of CDISC, Sponsor, and ICON standards.
- Collaborating with cross-functional teams to define data collection strategies and standards for clinical trials.
- Developing and maintaining training and reference materials related to standards topics including CDASH, SDTM, Terminology, ADaM, define-XML and regulatory submission requirements.
- Managing the development and maintenance of data management processes and tools.
- Keeping abreast of industry trends and regulatory updates related to data standards and ensuring their integration into ICON's practices.
Your profile
- A Bachelor's degree in a relevant field (e.g., Life Sciences, Computer Science, or related discipline); advanced degrees are a plus.
- Extensive experience in clinical data management and standards within the pharmaceutical or biotechnology industry.
- Advanced Proficiency in CDISC (Clinical Data Interchange Standards Consortium) standards and relevant regulations (e.g., FDA, EMA).
- Excellent analytical and problem-solving skills with a keen attention to detail.
- Excellent communication and collaboration abilities to work effectively in cross-functional teams.
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.
- 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.
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.
Principal Clinical Data Standards Consultant employer: ICON
Contact Detail:
ICON Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Clinical Data Standards Consultant
✨Tip Number 1
Familiarise yourself with CDISC standards and relevant regulations like FDA and EMA. Understanding these frameworks will not only help you in interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the clinical data management field. Attend industry conferences or webinars to connect with potential colleagues at ICON, which can give you insights into their work culture and expectations.
✨Tip Number 3
Prepare to discuss your experience with cross-functional teams. Highlight specific examples where you've collaborated on data collection strategies or developed training materials, as this is crucial for the role.
✨Tip Number 4
Stay updated on industry trends and regulatory changes. Being knowledgeable about recent developments will show your proactive approach and readiness to integrate new practices into ICON's operations.
We think you need these skills to ace Principal Clinical Data Standards Consultant
Some tips for your application 🫡
Understand the Role: Thoroughly read the job description for the Principal Clinical Data Standards Consultant position. Make sure you understand the key responsibilities and qualifications required, such as proficiency in CDISC standards and experience in clinical data management.
Tailor Your CV: Customise your CV to highlight relevant experience and skills that align with the job requirements. Emphasise your background in clinical data management, your analytical skills, and any specific projects that demonstrate your expertise in CDISC standards.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of ICON's mission. Use specific examples from your past experiences to illustrate how you can contribute to the team and the role.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial for the role you are applying for.
How to prepare for a job interview at ICON
✨Know Your CDISC Standards
As a Principal Clinical Data Standards Consultant, you'll need to demonstrate your advanced proficiency in CDISC standards. Brush up on the latest updates and be prepared to discuss how you've applied these standards in previous roles.
✨Showcase Your Analytical Skills
Highlight your analytical and problem-solving abilities during the interview. Be ready to provide examples of how you've tackled complex data challenges in clinical trials and the impact of your solutions.
✨Emphasise Collaboration Experience
Since the role involves working with cross-functional teams, share specific instances where you've successfully collaborated with others. Discuss how you defined data collection strategies and the outcomes of those collaborations.
✨Stay Updated on Industry Trends
Demonstrate your commitment to staying informed about industry trends and regulatory updates. Mention any recent changes in regulations that could affect data standards and how you would integrate these into ICON's practices.
