Global Clinical Data Lead – Senior Manager

ICON San Antonio; Warszawa; On-site; PLN 180,000 - 260,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance

Life assurance

Job summary

ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Senior Clinical Data Manager to lead data delivery across global trials. You will partner with sponsors to ensure regulatory-compliant data from startup through database lock, acting as the primary data lead on complex studies.

Responsibilities include EDC build, vendor oversight, data reconciliation, and risk mitigation while driving continuous improvement and operational excellence.

Qualifications

• Bachelor's degree in Life Sciences, Health Sciences, or a related discipline.
• 6+ years of Clinical Data Management or Clinical Data Science experience in CRO/pharma.
• Proven experience leading studies across the full clinical trial lifecycle.
• Experience as a primary Data Lead on complex studies and/or extensive data review and reconciliation across EDC, vendor, eCOA, IRT, and SAE data.

Responsibilities

• Acting as the primary data lead within cross-functional study teams and sponsor partnerships.
• Driving study start-up activities including EDC build, system integrations, UAT, and key data management deliverables.
• Overseeing data review, reconciliation, vendor management, and database lock activities.
• Ensuring compliance with CDISC standards, ICH-GCP requirements, and regulatory expectations.

Skills

Data management leadership

Cross-functional collaboration

Regulatory knowledge

Veeva EDC experience

Problem-solving

Project leadership

Education

Bachelor's degree in Life Sciences, Health Sciences, or related

Tools

Veeva EDC

EDC systems

eCOA data

Job description

ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Senior Clinical Data Manager to lead data delivery across global trials. You will partner with sponsors to ensure regulatory-compliant data from startup through database lock, acting as the primary data lead on complex studies.

Responsibilities include EDC build, vendor oversight, data reconciliation, and risk mitigation while driving continuous improvement and operational excellence.