<p>For one of our clients, an international pharma company in Basel, we are currently looking for a Data Quality Lead (m/f/d).<br /><br />In this role, you will lead the design, implementation, and oversight of 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.</p><p><br />General Information:<br /> </p><ul><li>Start date: June 2026</li><li>Latest start date: August 2026</li><li>Planned employment duration: 12 months with the possibility of extension</li><li>Contract: Temporary contract via Randstad</li><li>Workplace: Basel</li><li>Workload: 100%</li><li>Home Office: to be discussed</li><li>Working Hours: Standard</li></ul><p><br /> </p><p>Tasks & Responsibilities:</p><p> </p><ul><li>Operate as the core representative for Clinical Data Management on the study team and to be accountable for collection</li><li>Review and management of data and ensure deliverables are met</li><li>Leads the CDM study team and maintains oversight of all build, conduct and close activities for one or more studies, ensuring fit for purpose quality.</li><li>Implements study conventions, processes, knowledge sharing and best practices on assigned study(s)</li><li>Actively contribute to EDC system programming and maintenance.</li><li>Practical and theoretical expertise within his or her sub function.</li><li>In-depth understanding of the business of his or her sub function and the wider CDM organization.</li></ul><p><br /><br />Must Haves:<br /> </p><ul><li>BA/BS degree (or equivalent) coupled with moderate industry experience (3-5years) in a clinical research environment</li><li>In-depth understanding of CDM business processes and how they align with global regulatory requirements (GCDMP, ICH-GCP, etc.)</li><li>Expertise in ensuring data is "analysis-ready," requiring a theoretical and practical grasp of data flow from collection to submission</li><li>Proficiency in programming (e.g., SQL, SAS, or Python) to collaborate effectively with IT and drive system enhancements</li><li>Experience acting as the Primary Point of Contact (POC) & Leadership for CDM in cross-functional settings</li><li>Fluency in English written and verbal communication</li><li>Excellent presentation and communication skills are required</li></ul><p><br /><br />Nice to Haves:<br /> </p><ul><li>Vendor oversight and management experience</li></ul>