Data Quality Lead
Roche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a talented Data Quality Lead.
Background:
The Data Quality Lead will design, implement, and oversee data management activities across one or more studies. This includes database setup, data cleaning, query resolution, and vendor oversight, with a strong emphasis on regulatory compliance, efficiency, and data readiness for analysis. The role requires both technical acumen and collaborative leadership to anticipate challenges, drive process improvements, and enable high-quality data delivery across the clinical portfolio.
We seek a professional with proven capabilities in driving external vendors and partners to deliver high-quality databases. A strong programming background is essential for contributing effectively to EDC system development and maintenance in collaboration with IT.
Tasks & Responsibilities:
- Function as the core representative for Clinical Data Management on the study team and be accountable for data collection.
- Review and manage data to ensure all deliverables are met.
- Lead the Clinical Data Management study team and maintain oversight of all activities related to build, conduct, and closeout for one or more studies, ensuring fit for purpose quality.
- Implement study conventions, processes, knowledge sharing, and best practices on assigned studies.
- Actively contribute to EDC system programming and maintenance.
- Utilize practical and theoretical expertise within your subfunction.
- Exhibit programming and system development expertise along with an in-depth understanding of the broader Clinical Data Management organization.
Must Haves:
- A BA/BS degree (or equivalent) with moderate industry experience (3-5 years) in a clinical research environment.
- In-depth understanding of Clinical Data Management business processes and their alignment with global regulatory requirements (GCDMP, ICH-GCP, etc.).
- Expertise in ensuring data is "analysis-ready," requiring both theoretical and practical knowledge of the data flow from collection to submission.
- Proficiency in programming (e.g., SQL, SAS, or Python) to collaborate effectively with IT and drive system enhancements.
- Experience acting as the Primary Point of Contact (POC) and providing leadership for Clinical Data Management in cross-functional contexts.
- Fluency in English, both written and verbal communication skills.
- Excellent presentation and communication abilities are required.
Nice to Have:
- Experience in vendor oversight and management.
What You Will Be Offered:
- An opportunity to work in one of the world's most important pharmaceutical companies.
- A modern campus with plenty of green spaces and meeting areas.
- Central location in Basel.
- A varied job profile.
- Further training opportunities through Temptraining.
- Working in a dynamic and motivated team.
If you are interested, please apply online using the form below. Only applications matching the job profile will be considered.