Senior Lead Data Manager
Lead With Purpose. Protect the Integrity Behind the Science.
Since 1997, VCLS has supported BioTech, MedTech, and HealthTech innovators on their journey from discovery to patients. Our mission is simple and bold: accelerate life-changing products to market.
With 230+ experts worldwide, we are committed to a long-term vision: to help deliver 500 new healthtech products by 2050.
Behind every scientific breakthrough is data that can be trusted. Behind that trust is leadership. We are looking for a Senior Lead Data Manager who understands that Data Management is not just a function—it is a responsibility to patients, to science, and to the teams who rely on clarity and accuracy.
Why This Role Matters
This role is about impact through leadership.
As Senior Lead Data Manager, your influence extends beyond data quality. You will shape how Data Management evolves at VCLS—by developing people, sharing expertise, and guiding teams through change as we continue to invest in technology and capability.
Your experience will help bring clarity to complexity, strengthen ways of working, and ensure Data Management remains a trusted foundation for scientific decisions and patient impact.
What You Will Lead and Deliver
Lead With Clarity and Accountability
- Lead, supervise, and coordinate internal and outsourced Data Management teams.
- Set clear expectations and foster a culture of rigor, trust, and collaboration.
Champion Data Quality End-to-End
- Ensure high-quality, compliant clinical data throughout the full study lifecycle.
- Protect data integrity so that scientific and clinical decisions are made with confidence.
Advance CDISC Standards
- Implement and oversee CDISC standards (SDTM, ADaM) in close collaboration with Biostatistics.
- Ensure data structures support efficient analysis and regulatory expectations.
Shape the Tools That Shape the Data
- Contribute to the development of our in-house eCRF, including CDISC-compliant data structures designed for clarity and scalability.
Remain Hands-On
- Actively engage in data cleaning, validation, documentation, and review.
- Stay close to the work to strengthen both quality and leadership.
Improve How We Work
- Review, challenge, and enhance SOPs and Data Management processes with pragmatic, efficient solutions.
- Support implementation of new procedures, including training and onboarding of internal teams.
Optimize With Purpose
- Identify and implement workflow improvements aligned with industry best practices and CDISC standards.
Requirements
Who You Are
You are driven by curiosity, rigor, and a deep respect for the role data plays in patient outcomes.
- 5+ years of experience in Clinical Data Management within CROs, biotechs, or Life Science consulting organizations.
- Advanced expertise in CDISC standards (SDTM, ADaM).
- A confident leader with strong communication skills and a high standard for quality.
- Experienced in managing and constructively challenging external vendors.
- Fluent in English and comfortable working in an international environment.
Why Join VCLS
At VCLS, data is not an output—it is a foundation.
You will work alongside scientists, clinicians, and innovators who believe that rigor and humanity go hand in hand.
If you believe that great data enables great science—and that great science changes lives—we would love to hear from you.
Top Skills
What We Do
From discovery to product launch and lifecycle management
At VCLS (Voisin Consulting Life Sciences), regulatory science guides Biotechnology, Pharmaceutical and Medtech manufacturers throughout product development and commercialization. Starting early in the process, from discovery to the patient, VCLS assists innovators in designing optimized product development plans and regulatory strategies, combining the health ecosystem with commercial success. With a presence in seven locations across three continents and over 200 employees, VCLS serves a broad range of healthtech developers and their investors.
Together, we accompany global stakeholders to expedite HealthTech products from discovery to patient access and beyond by bridging Science to Regulatory and Market Access strategies.





