Data Quality Lead / Clinical Data Manager (m/f/d) – Basel
📋 Détails de l'offre
📖 Exigences
Expérience requise:
60 mois (5 ans)
60 mois (5 ans)
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About the role
For an international clinical development environment in Basel, we are looking for an experienced
Data Quality Lead / Clinical Data Manager
to support clinical studies across the full data management lifecycle.
In this role, you will take ownership of data management activities for one or more clinical studies, from database setup and EDC support through to data review, query management, vendor coordination and study closeout. The focus is on ensuring high-quality, compliant and analysis-ready clinical data while working closely with internal study teams, IT, external vendors and cross-functional stakeholders.
This position is ideal for a Clinical Data Management professional who combines strong regulatory understanding with solid technical capabilities, especially in areas such as EDC systems, data flow, programming and process optimisation.
General information
Start date:
1st to mid-June 2026
Latest start date:
1 August 2026
Duration:
12 months
Extension:
Likely, depending on project continuation
Workload:
100%
Location:
Basel
Home office:
To be discussed
Working hours:
Standard working hours
Team size:
Approx. 10–15 people
Department:
TDNC PDD Data Management
Main responsibilities
As Data Quality Lead / Clinical Data Manager, you will act as the central CDM representative within the study team and ensure reliable, compliant and timely data delivery.
Your responsibilities will include:
•
Leading Clinical Data Management activities for one or more assigned studies
•
Acting as the primary CDM point of contact for study teams and cross-functional partners
•
Overseeing database build, study conduct activities and closeout deliverables
•
Ensuring that clinical data is collected, reviewed, cleaned and managed according to study timelines
•
Driving data review, query resolution and issue follow-up to support analysis-ready datasets
•
Implementing study-specific conventions, standards, processes and best practices
•
Supporting knowledge sharing and continuous improvement within the CDM function
•
Contributing to EDC system programming, development, maintenance and optimisation
•
Collaborating with IT and technical teams on system enhancements and data-related requirements
•
Maintaining oversight of quality, compliance and deliverables across internal and external stakeholders
•
Supporting vendor coordination and follow-up where required
Required profile
You are an experienced Clinical Data Management professional with a strong understanding of clinical study data processes, regulatory expectations and technical system requirements.
You bring:
•
BA/BS degree or equivalent qualification
•
3–5 years of relevant experience in a clinical research or Clinical Data Management environment
•
Strong understanding of CDM processes and their alignment with global regulatory standards
•
Knowledge of GCDMP, ICH-GCP and related clinical data management requirements
•
Practical and theoretical understanding of data flow from collection through to analysis and submission
•
Experience ensuring clinical data is accurate, complete, consistent and analysis-ready
•
Good programming knowledge, for example in SQL, SAS or Python
•
Ability to collaborate with IT teams on EDC development, maintenance and system improvements
•
Background acting as a CDM primary point of contact in cross-functional study teams
•
Strong communication and stakeholder management skills
•
Fluent English skills, both written and spoken
•
Excellent presentation and communication abilities
Nice to have
•
Parcours professionnel with vendor oversight and external partner management
•
Previous expertise in a global pharmaceutical or biotech environment
•
Experience supporting multiple studies or complex clinical programmes
•
Strong ability to drive process improvements within Clinical Data Management
Ideal candidate
The ideal candidate is a confident Clinical Data Management professional who has already supported clinical studies from database build through to study closeout. You understand how high-quality clinical data is generated, reviewed and prepared for analysis, and you are comfortable working at the interface between study teams, IT, external vendors and data stakeholders.
You combine strong regulatory awareness with a hands-on technical mindset and are able to contribute not only to data management oversight, but also to EDC system development and process optimisation. Your communication style is clear, structured and professional, allowing you to act as a trusted CDM representative in cross-functional environments.
Manpower Basel
Herr Leroy Omokhuale
Recruiter
+4158 307 31 00
E-Mail schreiben
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🏢 À propos de l'entreprise
Entreprise dans le secteur Chimie / Pharma