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For Companies At a Glance
- Tasks: Lead the design and analysis of clinical trials while interpreting complex medical data.
- Company: Join ICON, a diverse team dedicated to advancing innovative treatments and therapies.
- Benefits: Enjoy competitive salary, health insurance, retirement planning, and flexible benefits.
- Why this job: Make a real impact in healthcare while collaborating with cross-functional teams in a supportive culture.
- Qualifications: Bachelor's degree in Life Sciences or related field; extensive experience in clinical data management required.
- Other info: Open to applications from across EMEA; advanced degrees and CDISC proficiency are a plus.
The predicted salary is between 43200 - 72000 £ per year.
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. We are happy to support applications from across EMEA.
What you will be doing
As a Senior Clinical Data Standards Consultant at ICON Plc, you will be responsible for:
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Developing tools to aid in the implementation and compliance of CDISC, Sponsor, and ICON standards.
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Collaborating with cross-functional teams to define data collection strategies and standards for clinical trials.
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Developing and maintaining training and reference materials related to standards topics including CDASH, SDTM, TermiNlogy, ADaM, define-XML and regulatory submission requirements.
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Managing the development and maintenance of data management processes and tools.
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Keeping abreast of industry trends and regulatory updates related to data standards and ensuring their integration into ICON’s practices.
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A Bachelor’s degree in a relevant field (e.g., Life Sciences, Computer Science, or related discipline); advanced degrees are a plus.
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Extensive experience in clinical data management and standards within the pharmaceutical or biotechNlogy industry.
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Advanced Proficiency in CDISC (Clinical Data Interchange Standards Consortium) standards and relevant regulations (e.g., FDA, EMA).
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Excellent analytical and problem-solving skills with a keen attention to detail.
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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.
Our benefits examples include:
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Various annual leave entitlements
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A range of health insurance offerings to suit you and your family’s needs.
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Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
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Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
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Life assurance
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Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
Principal Clinical Data Standards Consultant employer: ICON plc
Contact Detail:
ICON plc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Clinical Data Standards Consultant
✨Tip Number 1
Familiarize yourself with CDISC standards and relevant regulations like FDA and EMA. This knowledge is crucial for the role and will help you stand out during discussions.
✨Tip Number 2
Network with professionals in the clinical data management field. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends.
✨Tip Number 3
Showcase your analytical and problem-solving skills through real-world examples in conversations. Be prepared to discuss how you've tackled complex data challenges in previous roles.
✨Tip Number 4
Highlight your experience in cross-functional collaboration. Prepare to share specific instances where you've successfully worked with diverse teams to achieve common goals.
We think you need these skills to ace Principal Clinical Data Standards Consultant
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Principal Clinical Data Standards Consultant position. Understand the key responsibilities and required qualifications, as this will help you tailor your application effectively.
Highlight Relevant Experience: In your CV and cover letter, emphasize your extensive experience in clinical data management and standards, particularly with CDISC. Provide specific examples of how you've contributed to similar projects in the pharmaceutical or biotechnology industry.
Showcase Analytical Skills: Demonstrate your analytical and problem-solving skills in your application. Use concrete examples to illustrate how you've tackled complex data challenges in previous roles, as this is a crucial aspect of the job.
Tailor Your Communication: Since the role requires excellent communication and collaboration abilities, ensure that your application reflects your ability to work effectively in cross-functional teams. Mention any relevant experiences where you successfully collaborated with diverse groups.
How to prepare for a job interview at ICON plc
✨Showcase Your Expertise in CDISC Standards
Make sure to highlight your extensive experience with CDISC standards during the interview. Be prepared to discuss specific projects where you implemented these standards and how they contributed to the success of clinical trials.
✨Demonstrate Analytical Skills
Prepare examples that showcase your analytical and problem-solving skills. Discuss how you've tackled complex medical data and the impact of your solutions on clinical trial outcomes.
✨Emphasize Collaboration Experience
Since the role involves working with cross-functional teams, be ready to share experiences where you successfully collaborated with others. Highlight your communication skills and how they helped in defining data collection strategies.
✨Stay Updated on Industry Trends
Research recent trends and regulatory updates related to clinical data standards. Being knowledgeable about current developments will demonstrate your commitment to the field and your ability to integrate new practices into ICON's operations.
