Senior Clinical System Designer

Senior Clinical System Designer - Canada, Colombia, Mexico (Remote)
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are currently seeking a Senior Clinical System Designer to join ICON’s Full Service IOD Clinical Data Systems team. As a Senior Clinical System Designer at ICON, you will play a pivotal role in designing and implementing advanced clinical systems that enhance trial design and execution. Your expertise will be essential in driving innovation and ensuring that our clinical systems meet regulatory requirements and support operational efficiency.
Location: Remote or Hybrid
Canada
Mexico
Colombia
What you will be doing:
Leading the design and development of clinical systems, ensuring alignment with study protocols and operational needs
Consolidates and completes the high-level system requirements documents and manages their review
Responsible for copying and modifying CRFs from standard libraries and other studies
Provides support and review for the re-use of library items
Responsible for development of Custom CRF screens, Edit Check and Dynamic Check specification documents using prototyping methodologies as needed
Performs quality control peer reviews of database related specifications as needed and records comments appropriately
Lead eCRF and other specification review meetings
Ensures CDC review of edit check specifications
Utilizes edit checks from the appropriate library and modifies the library edit checks to meet trial specific requirements
Programs more complex dynamic checks and discrepancy edit checks to meet trial specific requirements
Review all activity on an ongoing basis to identify out of scope tasks and bring to the attention of the Clinical System Lead (CSL)
Support the CSL in negotiation of timelines and decision making on the study
Travel (approximately 10 %) domestic and/or international
Your profile:
5+ years of experience in the design and implementation of clinical systems within the clinical research industry
Expertise in data analysis and interpretation or Database Development, with proficiency in clinical data management systems and software
Knowledge of Medidata Rave or Veeva EDC
Excellent functional knowledge of CRF design tools and ability to plan and design CDMS components directly from interpretation of medium complexity clinical trial protocols
Excellent written and verbal communication skills
Bachelor’s Degree in a relevant field
* Please submit all applications in English *
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply

Skills
Data Analysis, Prototyping, Negotiation, Quality Control, Clinical Research