# Senior Clinical System Designer

**Company**: ICON
**Work arrangement**: remote
**Experience**: senior
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Colombia-Bogota/Senior-Clinical-System-Designer_JR158289?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
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## Description

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 Senior Clinical System Designer at ICON, you will design and implement 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 negotiating timelines and making decisions 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.

- Traveling approximately 10% domestically and/or internationally.

**Your Profile:**

- 3+ 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 one Clinical Data Management System (e.g., Medidata Rave, Veeva EDC).

- Excellent functional knowledge of Clinical Data Management CRF design tools and ability to plan and design CDMS components directly from interpreting medium-complexity clinical trial protocols.

- Excellent written and verbal communication skills.

- Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above.

- All employees must read, write, and speak fluent English and the host country language.

**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.

Benefits may vary depending on role and location.

## Skills

### Required
- Clinical Data Management Systems
- CRF design tools
- data analysis and interpretation
- database development
- English
- Spanish

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