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 *

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What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site (careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (careers.iconplc.com/reasonable-accommodation…)

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here (wd3.myworkday.com/icon/…) to apply