Senior Clinical Data Science Lead
- Warsaw, Johannesburg, Barcelona, Madrid
- Clinical Data Management, Data Science
- ICON Full Service & Corporate Support
- Hybrid: Office/Remote
About the role
This vacancy has now expired. Please see similar roles below...
With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
We have an fantastic opportunity for a Senior Clinical Data Science Lead to join ICON's Clinical Data Operations team.
LOCATIONS: home-based OR office-based
- Poland
- Spain
- Portugal
- United Kingdom
OVERVIEW OF THE ROLE:
The Senior Clinical Data Science Lead (Senior CDSL) serves as the primary contact for internal and external team members regarding clinical data science data review activities and leads these review activities to ensure delivery of data fit for analysis. They are accountable for achieving clinical data science deliverables on-time, with high-quality, and to agreed financial metrics.
- Develop and oversee timeliness of clinical data science activities during the life cycle of studies as it relates to data review and data delivery milestones
- Provide input into clinical system development activities and clinical risk management activities
- Track and keep functional management and those responsible for project management informed of any issues that might affect project target dates, scope or budget and escalates potential problems effectively and in a timely manner
- Forecast budget, hours, and resourcing for clinical data review activities
- Perform analytic review as defined in the scope of work and functional plans focusing on errors that matter or have a meaningful impact on the safety of the subject or interpretation of the final analysis
- Accountable for the development of planning documents related to data review, data analytics, and data deliverables.
- Participate in Sponsor and/or third-party audits.
- Negotiate timelines and key deliverables with clients and/or external customers, vendors, and departments as needed
- Travel (approximately 15%) domestic and/or international
TO BE SUCCESSFUL, YOU WILL NEED:
- 5+ years of clinical data management experience in a clinical research organization or pharmaceutical company
- 2+ years of experience working in a clinical research organization (CRO)
- Experience as a functional lead of multiple low and moderately complex studies, whilst acting as a resource for less experienced colleagues
- Experience with all steps within the data science lifecycle and most major data science study tasks, with proficiency in at least one Clinical Data Management system required (e.g., Medidata Rave, Inform, Oracle Clinical, Veeva)
- Excellent communication skills
- Budget and timeline management experience
- Data Analytic and Data Validation experience
- Bachelor’s degree or local equivalent
- Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above. All employees must read, write, and speak fluent English and host country language.
BENEFITS OF WORKING IN ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs.
In addition, our best-in-class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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 through the form below.
#LI-AH13
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. See all locations Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
10/02/2023
Summary
An Evolution of Progress and Success: Zashan's story a Clinical Research Associate (CRA) Having a satisfying career involves finding a company that prioritizes progress, improvement, and chances f
Teaser label
Our PeopleContent type
BlogsPublish date
08/22/2023
Summary
Skip to SAS Programming jobs What is SAS Programming? A statistical software suite called SAS for data management was established by the SAS Institute between 1966 and 1976 for the purposes
Teaser label
Our PeopleContent type
BlogsPublish date
05/19/2023
Summary
Skip to SAS Programming jobs What does a SAS programmer do? SAS programmers write, alter, and test the scripts and code that make it possible for applications to execute work from requi
Similar jobs at ICON
Salary
Location
India, Chennai
Location
Chennai
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Data Management
Data Science
Job Type
Permanent
Description
Functional Knowledge: •Good knowledge of clinical data science activities (Data review, risk management & analytics, clinical systems). •Working knowledge of project management, including the predicti
Reference
JR124697
Expiry date
01/01/0001
Author
Ekta Chandra SrivastavaAuthor
Ekta Chandra SrivastavaSalary
Location
London
Department
Biometrics Roles
Location
London
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Data Analytics
Job Type
Permanent
Description
The RBSM Central Risk plays a critical role contributing to the embedding, growth and continuous improvement of the clinical study risk management process. The RBSM Central Risk r is responsible for
Reference
2024-115203
Expiry date
01/01/0001
Author
Serena MilanesiAuthor
Serena Milanesi