Global Clinical Data Manager (Hybrid)

Join; Liestal; Hybrid; CHF 70.000 - 100.000; Vollzeit

Benefits dieser Stelle

Flexible working arrangements

Hybrid work options

Professional growth opportunities

Autonomy and responsibility

Collaborative team culture

Central location with good transport

Zusammenfassung

Join HEMEX AG seeks a Clinical Data Manager to lead data management for multinational trials in a hybrid Basel-Landschaft setting. You will design eCRFs, develop data management plans, and oversee data cleaning, QC, and SDTM derivations with R/Python support.

Collaboration across Clinical Ops, Pharmacovigilance, and Biostatistics is essential. The role requires a life sciences background with CRO/EDC experience, strong communication, and a high attention to detail.

Qualifikationen

• Fluent English (written and spoken) is required.
• Experience with EDC systems and clinical trial databases.
• Knowledge of CDISC standards (CDASH/SDTM) is preferred.
• Experience with MedDRA and WHODrug is advantageous.
• Strong data quality mindset and SOP compliance.

Aufgaben

• Plan, set up, conduct, clean, reconcile, and close databases for trials.
• Ensure data completeness, accuracy, traceability, and readiness for analysis.
• Collaborate with Clinical Ops, CRAs, Pharmacovigilance, Biostatistics, and sponsors.
• Translate protocols into eCRFs and maintain DS/Data Plans.
• Lead or coordinate UAT for EDC systems and ensure go-live readiness.
• Coordinate external data reconciliation and medical coding activities.

Kenntnisse

Fluent English

Strong communication

Organizational skills

Project coordination

Multitasking

Ausbildung

Bachelor's or Master's in Life Sciences or related

Tools

R programming

Python

Jobbeschreibung

Join HEMEX AG seeks a Clinical Data Manager to lead data management for multinational trials in a hybrid Basel-Landschaft setting. You will design eCRFs, develop data management plans, and oversee data cleaning, QC, and SDTM derivations with R/Python support.

Collaboration across Clinical Ops, Pharmacovigilance, and Biostatistics is essential. The role requires a life sciences background with CRO/EDC experience, strong communication, and a high attention to detail.