Senior Clinical System Designer
- Poland, South Africa
- Accounting & Finance
- ICON Strategic Solutions
- Remote
TA Business Partner
- Full Service Division
About the role
As a Senior Clinical System Designer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
- Provides technical solutions for data management deliverables in the data collection capability.
- Proactively engage in cross-functional EDC build Requirements, eCRF design meetings.
- Ensures eCRF is built according to the latest standards and best practices, including edit checks and applicable integrations (IWRS, CTMS, etc.); translate protocol requirements into optimal data capture approaches; either build and deploy a trial in an EDC system or oversee eCRF build and updates by CRO or vendor to confirm quality and consistency with standards.
- Responsible for QC on eCRF Forms/Fields, dynamics (DVRs/CFs), EDC integrations, etc., both on library and trial specific level;
- Ensure non-eCRF technologies for data capture (e.g., ePRO, safety reporting, coding, IWRS) are deployed as per requirements, including integrations with other systems, platforms or reporting environments with timelines for consumable data outlined.
- Creates tSDV technical specifications, Safety Gateway integration specifications and completes the Datamart mapping template.
- Responsible for acquiring and maintaining working knowledge in the various and future evolving data collection tools applied in the clinical trial space such as Medidata Rave.
- Support the development of eCRF standards and drive their implementation within the organization
You are:
- Bachelor’s degree or equivalent, in Computer Science or technical discipline with experience in clinical research.
- Technical Data Management experience.
- Technical Expertise in one or more of the following: eDC systems (Medidata, platform of tools), EDC integration tools, and general data capture platforms.
- Experience working on a clinical trial.
- Experience working in highly diverse teams within clinical research; cross-functional, global, multiregional.
- Project management skills.
- Highly organized with excellent written and verbal communication.
- Working knowledge of SDTM, including define.xml, CDASH, metadata and/or ADAM is an asset.
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 maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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 through the form below.
https://careers.iconplc.com/reasonable-accommodations
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.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
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Salary
Location
Poland
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Poland
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Accounting & Finance
Job Type
Permanent
Description
As a Senior Investigator Payment Coordinator, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-117237
Expiry date
01/01/0001
Author
Dagmara DrozdowskaAuthor
Dagmara Drozdowska