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
Career ProgressionContent type
BlogsPublish date
11/26/2025
Summary
How Clinical Research Job Seekers Can Enhance Their Applications Finding the right role in clinical research has become increasingly competitive as organisations continue to expand their study por
Teaser label
Inside ICONContent type
BlogsPublish date
11/14/2025
Summary
Building Bridges in Clinical Research: Daniela's Journey at ICON Daniela Rocco's career in clinical research has been driven by something straightforward but powerful: connection. From her e
Teaser label
Our PeopleContent type
BlogsPublish date
11/14/2025
Summary
Karina Espinoza's Journey at ICON Karina Espinoza's career in pharmacovigilance didn't begin with a grand plan. It started with a practical problem during her final year of a PhD in epidemiology, a
Similar jobs at ICON
Salary
Location
Turkey, Ankara
Location
Ankara
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
JR139905
Expiry date
01/01/0001
Author
Tuba SuAuthor
Tuba SuSalary
Location
Turkey, Ankara
Location
Ankara
Remote Working
Remote
Business Area
ICON Strategic Solutions
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
JR139900
Expiry date
01/01/0001
Author
Tuba SuAuthor
Tuba SuSalary
Location
Turkey, Ankara
Location
Ankara
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
JR139417
Expiry date
01/01/0001
Author
Tuba SuAuthor
Tuba SuSalary
Location
India, Chennai
Location
Chennai
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Senior Project Associate to join our diverse and dynamic team. As a Senior Project Associate at ICON, you will be responsible for assisting in the planning and execution of
Reference
JR135536
Expiry date
01/01/0001
Author
Himangshu Skekhar DasAuthor
Himangshu Skekhar DasSalary
Location
Mexico, Mexico City
Department
Clinical Monitoring
Location
Mexico City
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 Site Associate to join our diverse and dynamic team. As an CSA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials,
Reference
JR139034
Expiry date
01/01/0001
Author
Olivia MolinaAuthor
Olivia MolinaSalary
Location
UK, Reading
Location
Reading
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking an experienced (Cell & Gene Therapy) Clinical Research Associate to partner one of the top 5 Global Pharmaceutical companies. As a Clinical Research Associate at ICON, you wil
Reference
JR137601
Expiry date
01/01/0001
Author
Dominic BradyAuthor
Dominic Brady