Analytics Development Lead
About the role
This vacancy has now expired. Please click here to view live vacancies.
Role summary
We are looking to recruit an Analytics Development Lead as part of a specialist team responsible for building derived data libraries, Data Quality Assessment (DQA) and Key Risk Indicator (KRI) dashboards in the central monitoring platform CluePoints.com, as well as performing KRI and DQA analysis in the platform to support central monitoring.
The candidate will be working with stakeholders to define study level Risk-Rased Monitoring (RBM) strategies, hands-on deployment, processing and maintenance of data for analysis and process documentation. This position will also be expected to conduct central monitoring activities, such as system output review, signal reporting and action management. Mentorship of junior technical staff is expected and the ability to work both independently and in a matrix team environment is essential.
*This role can be based in Dublin or Warsaw*
Key responsibilities:
- Develop and maintain study set-up in the central monitoring platform
- Define and build KRIs, ensuring standard deployment consistency and alignment with corporate standards and regulatory requirements
- Build and maintain study specific DQA dashboard, analyse and report any data quality outliers and atypicality
- Influence and communicate with key stakeholders and provide data reporting support to study teams across the research and business units
- Build and maintain collaborative working relationships with stakeholders to review reported findings, actions resolution and solve problems as and when they arise.
- Provide technical oversight, guidance and coordination for all the central monitor activities
- Implement and maintain quality control (QC) documentation for RBM activities, in accordance with departmental procedures
- Manage own time and priorities effectively while working on multiple projects
- Mentor and supervise less junior staff and be responsible for the quality and accuracy of the work done
Key Responsibilities:
- Bachelor's degree, or equivalent level qualification in Natural Sciences, Mathematics, Computer Science, Information Management or Information Technology, or have gained experience in a similar discipline.
- Experience in developing in R, SAS or any other SQL languages
- Knowledge of Windows Environment and its applications (Word, Excel, PowerPoint, Project, etc.)
- Good understanding of data modelling and manipulation techniques, including ETL and aggregation methods
- Project management experience and proven business analysis and requirements elicitation skills
- Good presentation skills and proven ability communicating requirements and solutions to team members and stakeholder
- Working knowledge of clinical development process and good understanding of clinical data management
- Desired experience in clinical risk management, central monitoring strategies and statistics-based data profiling
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
01/26/2026
Summary
Sometimes the best way to recognise what you have is to experience life without it. For Izabella Grimaldi, a Clinical Research Associate II based in Brazil, that realisation came after seven months wo
Teaser label
IndustryContent type
BlogsPublish date
01/20/2026
Summary
Understanding the Difference Between CRA, CTA, and SMA Clinical research job titles can be confusing, particularly for those new to the industry. Acronyms such as CRA, CTA and SMA appear frequentl
Teaser label
Inside ICONContent type
BlogsPublish date
01/05/2026
Summary
Interviewing at ICON: What to Expect Applying for a new role can feel uncertain, particularly when recruitment processes use digital tools or assessments that may be unfamiliar. At ICON, we want ca
Similar jobs at ICON
Salary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Data Science Programmer to join our diverse and dynamic team. As a Senior Clinical Data Science Programmer at ICON, you will play a pivotal role in developin
Reference
JR142972
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Canada, Burlington
Location
Burlington
Calgary
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical
Reference
JR142797
Expiry date
01/01/0001
Author
Brendan HoeyAuthor
Brendan HoeySalary
Location
Mexico, Mexico City
Department
Full Service - Development & Commercialisation Solutions
Location
Mexico City
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Data Management
Analyst
Job Type
Permanent
Description
Medical Imaging - Data Analyst I Home based What You Will Be Doing:Primary responsibilities include management of data analysis and data quality control of Independent Read data based on Post Read QC
Reference
JR139194
Expiry date
01/01/0001
Author
Daniela GuerreroAuthor
Daniela GuerreroSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
Lead, Site ResourcingWhat You Will Be Doing:Leading day-to-day site resourcing activities, including the allocation of CRAs, site managers, and other site-facing roles to studies.Collaborating with pr
Reference
JR136980
Expiry date
01/01/0001
Author
Daniela GuerreroAuthor
Daniela GuerreroSalary
Location
Italy, Milan
Department
Clinical Monitoring
Location
Milan
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Clinical Site Associate (CSA)We are currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team. As a CSA at ICON, you will play a pivotal role in supporting clinical trial
Reference
JR142035
Expiry date
01/01/0001
Author
Sophie BinghamAuthor
Sophie BinghamSalary
Location
Spain, Madrid
Department
Clinical Monitoring
Location
Barcelona
Madrid
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli
Reference
JR142950
Expiry date
01/01/0001
Author
Lourdes Roy PratsAuthor
Lourdes Roy Prats