Associate Clinical System Designer

ICON is seeking an Associate Clinical System Designer to join its 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.

Responsibilities:

• 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.
• Copy and modify 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
• 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 escalate potential problems effectively and in a timely manner
• With support, consolidate and complete high-level system requirements documents and facilitate their review
• With support, perform quality control peer reviews of database related specifications as needed and record comments appropriately
• Support more senior project leads in performing eCRF and other specification review meetings
• Support simple to medium migration/post-production change activities
• Assist with EDC integration related activities

Requirements:

• 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

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