Clinical Data Engineer

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

The Clinical Data Enablement Manager(FSP) is responsible for supporting the operation and

continuous improvement of clinical data pipelines across cloud-based data lake and data warehouse

environments. This role executes defined ingestion and transformation processes, assists with

monitoring and troubleshooting, collaborates with internal teams and external vendors, and helps

ensure timely, high-quality, and compliant delivery of clinical data outputs to downstream users.

What You Will Do:

. Support end-to-end clinical data pipelines across lake/warehouse environments (build, run, monitor, maintain, troubleshoot) to ensure stable, traceable operations.

• Assist with operational support activities including monitoring/alerting, incident triage, root cause analysis support, and implementing corrective/preventive actions under guidance.

• Develop and enhance cloud ETL/ELT pipelines (AWS/Azure) for ingestion, transformation, and delivery, following established patterns and standards.

• Implement automation for scheduling, repeatable ingestion, and automated quality checks to improve reliability and timeliness.

• Design, develop, and maintain operational dashboards and data visualizations using approved platforms to support pipeline health monitoring, data quality oversight, and operational reporting for stakeholders.

• Support vendor and cross-functional integrations by implementing data transfers per specifications, performing validation/reconciliation, and escalating issues as needed.

• Collaborate with downstream teams (Stat Programming, SDTM, Analytics, Clinical Data Programming) to understand data needs and deliver required datasets/exports (format, structure, cadence).

• Contribute to on-time, high-quality delivery against agreed specifications and participate in tracking and reporting operational KPIs (e.g., timeliness, success rate, defects) through dashboards and metrics.

• Follow controlled documentation and change practices for regulated clinical processes; support GxP/CSV activities by maintaining required documentation, test evidence, and traceability as assigned.

• Apply data integrity practices (e.g., ALCOA+ expectations per internal standards) and adhere to access controls and audit trail/logging requirements in collaboration with Quality/Compliance/IT.

Required qualifications and experience

• Education/Experience: BS/BA (or equivalent) plus 5+ years in data engineering, pipeline development/operations, and multi-source data integration (clinical/biopharma preferred).

• Core skills: Foundational SQL skills; understanding of basic data modeling and data quality checks; familiarity with integration patterns (NoSQL exposure a plus).

• Programming/SDLC: Proficiency in Python (preferred) or R; exposure to building/supporting pipelines with basic testing, logging, and monitoring; familiarity with Agile/SDLC concepts; Jira/Confluence experience preferred (or ability to learn quickly).

• Visualization & Reporting (for Reporting role): Hands-on experience designing and supporting operational dashboards and data visualizations using tools such as Power BI, Tableau, and/or QlikView, with an understanding of data refresh, access controls, and performance considerations.

• Data standards (preferred): Awareness of CDISC/CDASH/SDTM concepts and willingness to learn how standards impact downstream clinical deliverables.

• Data formats & Interfaces: Hands-on with CSV, JSON, XML and file/API-based integrations; able to follow transfer specifications and validate outputs.

• Cloud/platforms (preferred): Exposure to AWS and/or Azure and modern data platforms (e.g., Snowflake, Databricks, Spark); ability to implement within established frameworks and standards. • DevOps: Working knowledge of GitHub/GitLab version control; CI/CD exposure is a plus.

• GxP & Data integrity (preferred): Experience or exposure to GxP-regulated practices (documentation, change control, audit readiness) and understanding of data integrity expectations; able to follow controlled procedures and maintain required evidence.

• Ways of working / working style: Strong collaboration and communication; organized, detailoriented, proactive; able to prioritize tasks, follow guidance, and deliver to deadlines in a fast-paced environment.

• Preferred: Prior regulatory inspection/audit support experience; AWS/Azure and/or Python certification.

Preferred qualifications and experience

Advanced Python or R, SQL and understanding of clinical data standards are mandatory requirements.

• Relevant experience includes building data pipelines using AWS services (EMR, S3, Glue, RDS) and hands-on experience with pipeline development and deployment using CI/CD and GitHub Actions.
• Current integrations are primarily file-based (SFTP) with Databricks/ Delta Lake
• Primary clinical data platforms for integration are Veeva CDB and Elluminate/JReview.
• Tableau is the preferred strategic data visualization tool.
• Candidates should be able to troubleshoot data-transfer issues and communicate effectively with business and downstream stakeholders.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• 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.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

About Us

ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live.

If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.