P2617 - Senior Clinical Data Manager — Debiopharm
- Location
- Lausanne
- Contract
- other
- Posted
- 70 days ago
Role overview
Together, we innovate, we impact, we grow At Debiopharm, every step we take is guided by one purpose: improving the lives of people affected by cancer and infectious diseases.
As a privately-owned Swiss biopharmaceutical company, we’re driven by science, but above all, by the people behind every treatment — the patients and their families.
Through our unique “development only” model, we bring forward promising therapies and transform them into treatments that can reach those who need them most, faster.
- Together, we innovate, we impact, we grow At Debiopharm, every step we take is guided by one purpose: improving the lives of people affected by cancer and infectious diseases.
- As a privately-owned Swiss biopharmaceutical company, we’re driven by science, but above all, by the people behind every treatment — the patients and their families.
- Requirements
- Education: Scientific or technical background, ideally at a university level.
- Education: Scientific or technical background, ideally at a university level. In addition, any Project Management certification would be a plus.
- Experience: At least 10 years in clinical data management, working in matrix organization with at least one previous and solid experience in pharmaceutical industry and supporting Phase 1 to 3 studies. Project Management experience, an asset.
Main responsibilities
- Requirements
- Education: Scientific or technical background, ideally at a university level.
- In addition, any Project Management certification would be a plus.
Key requirements
- Education: Scientific or technical background, ideally at a university level. In addition, any Project Management certification would be a plus.
- Experience: At least 10 years in clinical data management, working in matrix organization with at least one previous and solid experience in pharmaceutical industry and supporting Phase 1 to 3 studies. Project Management experience, an asset.
- Technical Expertise: Strong experience with various EDC systems and first experience or proficiency automating activities with AI.
- Leadership: Proven track record in leading data management studies and teams to deliver high-quality, regulatory-compliant databases.
- Skills: Excellent organizational, planning/coordination, proactivity and communication skills. Tech savvy, especially with Digital tools and AI
- Languages: Fluent in English; knowledge of French is a distinct asset.
What the company offers
- Being part of a company where innovation, collaboration, and impact aren’t just values — they’re how we work every day
- Partner with teams across disciplines, at the forefront of oncology and anti-infective development
- An inclusive and respectful workplace — proud to be Equal-Pay certified
- Grow in a culture that values people, purpose, and performance A chance to grow, share, and shape the future of healthcare
Company and context
- Experience: At least 10 years in clinical data management, working in matrix organization with at least one previous and solid experience in pharmaceutical industry and supporting Phase 1 to 3 studies.
- Project Management experience, an asset.
- Technical Expertise: Strong experience with various EDC systems and first experience or proficiency automating activities with AI.
- Leadership: Proven track record in leading data management studies and teams to deliver high-quality, regulatory-compliant databases.
- Skills: Excellent organizational, planning/coordination, proactivity and communication skills.
- Tech savvy, especially with Digital tools and AI
- Languages: Fluent in English; knowledge of French is a distinct asset.
Additional details
- Grow in a culture that values people, purpose, and performance A chance to grow, share, and shape the future of healthcare
Notes and original content
- Responsibilities
- Grow in a culture that values people, purpose, and performance
- A chance to grow, share, and shape the future of healthcare
Questions about this listing
What salary does Debiopharm offer for this role?
Debiopharm lists CHF 95'000 - 132'500 gross per year for this position in Lausanne. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Debiopharm offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Debiopharm during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Vaud?
EU/EFTA residents living in the border zone of the country adjoining Canton Vaud can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Vaud's cantonal migration office or with HR during the application.
How do I apply for this position at Debiopharm?
Use the "Apply now" button on this page — it links directly to Debiopharm's original listing at apply.workable.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
