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
02/05/2026
Summary
Building expertise through diverse roles and continuous learning Sinéad McKeon's career at ICON demonstrates how scientific training can evolve into strategic leadership. Now a Senior Manager in Lab
Teaser label
Our PeopleContent type
BlogsPublish date
02/05/2026
Summary
Shaping the Future of Patient Safety At ICON, patient safety is the foundation of everything we do. Hassan Aljobori, Director of Pharmacovigilance, shares his journey through nine years of growth
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
Similar jobs at ICON
Salary
Location
UK, South London (Accellacare)
Department
Accellacare Site Network
Location
London
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Research Site Services
Job Type
Permanent
Description
We are currently seeking a CRC Level 1 to join our diverse and dynamic team. As a CRC Level 1 at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex med
Reference
JR138729
Expiry date
01/01/0001
Author
Lourdes Roy PratsAuthor
Lourdes Roy PratsSalary
Location
UK, Northhamptonshire (Accellacare)
Department
Accellacare Site Network
Location
Northhamptonshire
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Research Site Services
Job Type
Permanent
Description
We are currently seeking a CRC Level 1 to join our diverse and dynamic team. As a CRC Level 1 at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex med
Reference
JR138383
Expiry date
01/01/0001
Author
Lourdes Roy PratsAuthor
Lourdes Roy PratsSalary
Location
Japan, Tokyo
Department
Clinical Monitoring
Real World Solutions
Location
Osaka
Tokyo
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
現在、当社の多様でダイナミックなチームに加わっていただける治験実施施設管理担当者を募集しています。ICONの施設管理担当者として、施設管理チームに運営上のサポートを提供し、治験の円滑な運営と革新的な治療法の進歩に貢献する重要な役割を担っていただきます。職務内容 ・治験実施施設訪問のスケジュール設定、会議資料の準備、治験文書の保管など、治験実施施設の管理活動の調整を支援します。 ・施設管理計画の策定
Reference
JR139358
Expiry date
01/01/0001
Author
Aoi HayashidaAuthor
Aoi HayashidaSalary
Location
Japan, Tokyo
Department
Clinical Monitoring
Real World Solutions
Location
Osaka
Tokyo
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
現在、当社の多様でダイナミックなチームに加わっていただける治験実施施設管理担当者を募集しています。ICONの施設管理担当者として、施設管理チームに運営上のサポートを提供し、治験の円滑な運営と革新的な治療法の進歩に貢献する重要な役割を担っていただきます。職務内容 ・治験実施施設訪問のスケジュール設定、会議資料の準備、治験文書の保管など、治験実施施設の管理活動の調整を支援します。 ・施設管理計画の策定
Reference
JR139350
Expiry date
01/01/0001
Author
Aoi HayashidaAuthor
Aoi HayashidaSalary
Location
Japan, Tokyo
Department
Clinical Monitoring
Location
Osaka
Tokyo
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking an IHCRA (In-House Clinical Research Associate) to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and managem
Reference
JR139356
Expiry date
01/01/0001
Author
Aoi HayashidaAuthor
Aoi HayashidaSalary
Location
India, Chennai
Department
Full Service - Corporate Support
Location
Chennai
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Accounting & Finance
Job Type
Permanent
Description
We are currently seeking a Senior Financial Accountant to join our diverse and dynamic team. As a Senior Financial Accountant at ICON, you will ensure accurate financial reporting, compliance with reg
Reference
JR139550
Expiry date
01/01/0001
Author
Puja JaiswalAuthor
Puja Jaiswal