Associate Clinical System Designer

Associate Clinical System Designer - United States, Canada, Mexico, Colombia
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 an Associate Clinical System Designer to join ICON’s Full-Service IOD Clinical Data Science team. As an Associate Clinical System Designer at ICON, you will play a pivotal role in designing and implementing advanced clinical systems that enhance trial design and execution.
Locations:
Mexico City (Office-Based Hybrid)
Blue Bell, USA (Office-Based Hybrid)
Raleigh, NC (Office-Based Hybrid)
Colombia (Remote)
Canada (Remote)
What you will be doing:
Assist with development of Custom CRF screens, Edit Check, and Dynamic Check specification documents, using prototyping methodologies as needed
Assist with the creation of technical specifications for output programming such as Data Validation Outputs, Data Analytics outputs, custom output programs etc.
Copies and modifies CRFs from standard libraries and other studies under specific instruction
Read, ensure understanding and adhere to the study protocol, contract and scope of work for all tasks during set-up, maintenance and close-out of the study
Tracks and keeps 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
With support, consolidates and completes the high-level system requirements documents and facilitates their review
With support, performs quality control peer reviews of database related specifications as needed and records comments appropriately
Supports more senior project leads in performing eCRF and other specification review meetings
Supports for simple to medium migration/post-production change activities
Assist with the EDC integration related activities
Your profile:
6+ months 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
Experience with Medidata Rave and/or Veeva EDC
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 *
#LI-TP1
#LI-Hybrid
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, Project Management, Prototyping, Quality Control, Clinical Research