Associate Clinical System Designer
ICON plc
Summary
ICON is 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.
Job description
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
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
- Proficiency in clinical data management systems and software
- Experience with Medidata Rave and/or Veeva EDC
- Functional knowledge of CRF design tools
- Ability to plan and design CDMS components from interpretation of medium complexity clinical trial protocols
- Excellent written and verbal communication skills
- Bachelor's Degree in a relevant field
Benefits
- Competitive Base Salary
- Performance Incentives
- Medical, Dental & Vision
- Retirement & Pension Plans
- Life Assurance
- Disability Coverage
- Employee Assistance Programme
- Wellbeing Resources
- Learning & Development
Company overview
ICON plc is a global leader in clinical research and healthcare intelligence, founded in Dublin, Ireland in 1990. As one of the world's largest contract research organizations (CROs), ICON provides comprehensive outsourced development services to pharmaceutical, biotechnology, and medical device companies worldwide. The company operates in 55 countries with approximately 41,900 employees, offering end-to-end solutions that span the entire product development lifecycle. ICON's service portfolio includes clinical research services, adaptive trials, biosimilars, commercialization and outcomes consulting, medical imaging, laboratory services, and strategic support for traditional and digital health technologies. The company specializes in therapeutic areas such as oncology, cardiovascular diseases, central nervous system disorders, rare diseases, and women's health. With its 2021 acquisition of PRA Health Sciences, ICON significantly expanded its capabilities and market position, becoming a dominant force in the global CRO industry. The company is publicly traded on NASDAQ under the ticker ICLR and reported $8.28 billion in revenue for 2024.