About the Role
We are seeking an experienced Clinical Data Lead to join our team in Basel, to oversee clinical data management for ongoing and upcoming trials. You will take responsibility for data management strategy, execution and delivery — from database build to final database lock — ensuring data quality, compliance and timely delivery to internal/external stakeholders.
Key Responsibilities
* Act as the main point of contact for data management deliverables sponsor / CRO / internal stakeholders.
* Develop, review and maintain data management documentation — e.g., Data Management Plans (DMPs), CRF specifications, data validation specifications, user access rights, SOPs/work instructions, oversight and QC procedures.
* Oversee, mentor or coordinate junior data team members / contractors as needed, supporting quality delivery and adherence to timelines.
* Ensure data management processes comply with applicable clinical trial regulations, Good Clinical Practice (GCP) guidelines, and audit/inspection readiness requirements.
* Collaborate cross‑functionally (clinical operations, biostatistics, regulatory, safety, laboratories) to support trial execution, data flow, integration and final deliverables.
Requirements
* 5+ years in clinical data management /clinical research, ideally in a CRO or Biotech environment.
* Strong knowledge of clinical trial data lifecycle, EDC systems CRF design, data validation/cleaning, database lock, data QC and documentation.
* Familiarity with regulatory guidelines and GCP compliance; ability to maintain audit‑ready data deliverables.
Seniority Level
* Mid-Senior level
Employment Type
* Contract
Job Function
* Analyst
Industries
* Pharmaceutical Manufacturing and Biotechnology Research
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