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For Companies At a Glance
- Tasks: Design and analyze clinical trials, interpret medical data, and develop compliance tools.
- Company: ICON plc is a leading healthcare intelligence and clinical research organization.
- Benefits: Enjoy competitive salary, health insurance, retirement planning, and flexible benefits.
- Why this job: Join a diverse team driving innovation in clinical development and making a real impact.
- Qualifications: Bachelor's degree in relevant field; experience in clinical data management and CDISC standards required.
- Other info: ICON values diversity and inclusion, offering equal opportunities for all applicants.
The predicted salary is between 43200 - 72000 £ per year.
Principal Clinical Data Standards Consultant
Principal Clinical Data Standards Consultant – India, Bangalore
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, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We’re proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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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Principal Clinical Data Standards Consultant employer: ENGINEERINGUK
Contact Detail:
ENGINEERINGUK 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 collaboration experience with cross-functional teams. Share specific instances where your communication skills led to successful project outcomes.
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, especially focusing on CDISC standards and clinical data management.
Tailor Your CV: Customize your CV to highlight relevant experience in clinical data management and your proficiency with CDISC standards. Use specific examples that demonstrate your analytical skills and attention to detail.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for clinical research and innovation. Mention how your background aligns with ICON's mission and values.
Highlight Collaboration Skills: Since the role involves working with cross-functional teams, emphasize your communication and collaboration abilities in both your CV and cover letter. Provide examples of successful teamwork in previous roles.
How to prepare for a job interview at ENGINEERINGUK
✨Understand CDISC Standards
Make sure you have a solid grasp of CDISC standards, including CDASH, SDTM, and ADaM. Be prepared to discuss how you've applied these standards in your previous roles and how they can impact clinical trial design.
✨Showcase Analytical Skills
Prepare examples that highlight your analytical and problem-solving skills. Discuss specific challenges you've faced in clinical data management and how you overcame them, emphasizing your attention to detail.
✨Emphasize Collaboration Experience
Since the role involves working with cross-functional teams, be ready to share experiences where you've successfully collaborated with others. Highlight your communication skills and how they contributed to achieving project goals.
✨Stay Updated on Industry Trends
Demonstrate your knowledge of current industry trends and regulatory updates related to data standards. Discuss how you keep yourself informed and how you would integrate this knowledge into ICON's practices.
