Data Quality Lead (m/f/d): Clinical Research / CDM / GCDMP / ICH-GCP / SQL / SAS / Python / English
Project
For our client based in Basel, we are looking for a Data Quality Lead.
Background
The Data Manager leads 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. The candidate must have proven capabilities in driving external vendors and partners in delivering high quality databases, and strong programming skills to contribute effectively to EDC system development and maintenance.
The Perfect Candidate
A seasoned Clinical Data Management professional with a BA/BS degree and 3‑5 years of experience leading study teams from database build to closeout. The candidate should blend deep regulatory knowledge of ICH‑GCP with technical proficiency in SQL, SAS, or Python to ensure data is "analysis‑ready" and systems are optimised. The role demands a high‑impact primary point of contact, bridging technical EDC development and cross‑functional clinical leadership with fluent communication.
Tasks & Responsibilities
* Operate as the core representative for Clinical Data Management on the study team and be accountable for data collection.
* Review and manage data to ensure deliverables are met.
* Lead the CDM study team and maintain oversight of all build, conduct and close activities for one or more studies, ensuring fit‑for‑purpose quality.
* Implement study conventions, processes, knowledge sharing and best practices on assigned study(s).
* Actively contribute to EDC system programming and maintenance.
* Apply practical and theoretical expertise within the sub function.
* Provide programming and system development expertise and an in‑depth understanding of the business and the wider CDM organisation.
Must Haves
* BA/BS degree (or equivalent) coupled with moderate industry experience (3‑5 years) in a clinical research environment.
* In‑depth understanding of CDM business processes and how they align with global regulatory requirements (GCDMP, ICH‑GCP, etc.).
* Expertise in ensuring data is "analysis‑ready," requiring a theoretical and practical grasp of 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 leadership for CDM in cross‑functional settings.
* Fluency in English, written and verbal communication.
* Excellent presentation and communication skills.
Nice to Haves
* Vendor oversight and management experience.
Job Details
* Reference Nr.: 924917
* Role: Data Quality Lead (m/f/d)
* Industry: Pharma
* Location: Basel
* Pensum: 100%
* Start: 1st June
* Latest possible start date: 01.08.2026
* Duration: 12+ Months
* Deadline: 06/05/2026
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