# Senior Clinical System Designer

**Company**: ICON
**Location**: Canada (Remote)
**Work arrangement**: remote
**Experience**: senior
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Canada-Burlington/Senior-Clinical-System-Designer_JR156588?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_b924ec73-674

## Description

ICON is seeking a Senior Clinical System Designer to join its Full-Service IOD Clinical Data Science 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.

**Responsibilities:**

- Leading the design and development of clinical systems, ensuring alignment with study protocols and operational needs

- Consolidating and completing high-level system requirements documents and managing their review

- Copying and modifying CRFs from standard libraries and other studies

- Providing support and review for the re-use of library items

- Developing custom CRF screens, Edit Check and Dynamic Check specification documents using prototyping methodologies as needed

- Performing quality control peer reviews of database related specifications as needed and recording comments appropriately

- Leading eCRF and other specification review meetings

- Utilizing edit checks from the appropriate library and modifying them to meet trial specific requirements

- Programming more complex dynamic checks and discrepancy edit checks to meet trial specific requirements

- Reviewing all activity on an ongoing basis to identify out of scope tasks and bringing them to the attention of the CSL

- Supporting the CSL in negotiation of timelines and decision making on the study

- Assisting in assessing impacts of post-production database related changes and compiling change management documentation for review by project team leads

- Driving post-production database changes and releasing them into production

- Travelling approximately 10% domestically and/or internationally

**Requirements:**

- 5+ years of experience in designing and implementing 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 at least 1 Clinical Data Management System (e.g. Medidata Rave, 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

**Rewards & Benefits:**

- 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

## Skills

### Required
- Clinical Data Management Systems
- CRF design tools
- Database Development
- Data analysis and interpretation

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