Clinical Research Associate
This role involves monitoring clinical trials and ensuring protocol compliance and data integrity. ICON offers career development, a collaborative environment, and various well-being benefits.
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88,000+ live jobsRemote, Germany, Frankfurt·Added 3 months ago
This job was published 3 months ago
Permanent contract
Per the ad.
Fully remote
Per the ad.
Have the right to work in Spain
ICON plc doesn't mention sponsorship in the ad.
Work in English
English is required, per the ad.
Have 5+ years of experience
Mid-level role.
University degree
“An undergraduate degree or international equivalent from an accredited institution” — per the ad.
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:
• Minimum of 5 years of experience in industry in a role demonstrating knowledge of clinical data standards used by biometrics.
• Demonstrated expertise in CDASH, SDTM standards and associated controlled terminology with a good understanding of CRF design concepts.
• Excellent communication skills with demonstrated leadership ability.
• An undergraduate degree or international equivalent from an accredited institution
Clinical Data Standards Consultant - ADaM
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.
Job Advert Posting
A Clinical Data Standards Consultant is responsible for supporting the operational staff in the use of ADaM and the define.xml capture for statistical analysis within the Medidata standard. They will develop tools to increase the efficiency, timeliness and quality of deliverables for data collection, tabulation, analysis and reporting. They will also define and collect metrics about the use of standards. They will participate in the development of training of the operational staff in the areas of their expertise.
Serve on Sponsor Standards and Technology Leadership teams.
Consult with clients on sponsor-specific CDISC centric implementation projects.
Participate in industry groups focused on the development of standards related initiatives (e.g. CDISC, PhUSE etc.).
Author, maintain, implement, and report status for Standards Related Project Plans.
Responsible for the implementation, strategy, and configuration of a metadata repository used to manage libraries of CDISC related metadata, terminology and related standards.
Mentor Clinical Data Standards Consultants. * Lead Subject Matter Expert teams on topics relevant to standards.
Identify areas for process improvement which may increase productivity, quality and / or compliance of deliverables in the areas from data collections through analysis and reporting.
Participate in the analysis of metrics and in creating recommendations to the management teams on process improvements together with the Director of Global Data Standards.
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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
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
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