P2617 - Senior Clinical Data Manager
Listed on 2026-09-13
-
Management
Regulatory Compliance Specialist
Together, we innovate, we impact, we grow
AtDebiopharm, 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'redriven by science, butabove all, bythe 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.
Are you passionate about advancing science and improving lives?
We are currently looking for adriven,passionateandcollaborativeprofessionalto join our Biostatistics and Data Management department based at our Headquarters in Lausanne, Switzerland as
Permanent role |
Location:
Lausanne, Switzerland
As aSenior Clinical Data Manager, you will be accountable for the quality and timelines of data management activities across assigned clinical studies. You will play a pivotal role in ensuring that complete,accurate, and consistent clinical data is available to support our internal decision-making processes.
Whether managing internal tasks or overseeing activities outsourced to external providers, you are the guardian of data integrity and quality.
- Study Leadership:Lead andcoordinateCDMactivities,includingeCRFdesign, EDC system setup, User Acceptance Testing(UAT), anddatabaserelease.
- Operational Excellence:Performdatareview,querygeneration, and datacodingwhileensuringtimelydata capturefrombothinternalandexternalsources.
- Strategic Planning:Define andmanagetimelines for multiplestudiesordevelopmentprograms.
- Documentation &Compliance:Prepareandreview Data Management Plans (DMP) and validation plans in strict compliancewithGCP, SOPs, andregulatoryguidelines.
- Lifecycle Management:Overseethe lock,transfer, andarchivingofclinicalstudydatabases.
- Collaboration:Actasakeymemberof theclinicalstudyteam,workingcloselywith
Clinical
Trial Managers andotherstakeholders inamatrixenvironment.
Your profile
- Education:Scientific ortechnicalbackground,ideallyat auniversitylevel. In addition, any Project Management certification would be a plus.
- Experience:At least
10 years inclinicaldata management,workingin matrixorganizationwith at least onepreviousandsolidexperiencein pharmaceutical industry and supporting Phase1 to3 studies.
Project Management experience, anasset. - Technical Expertise:StrongexperiencewithvariousEDCsystemsand first experience orproficiencyautomating activities with AI.
- Leadership:Proventrackrecord inleadingdatamanagementstudiesandteamstodeliverhigh-quality,regulatory-compliantdatabases.
- Skills:Excellent organizational, planning/coordination,proactivity and communication skills.
Techsavvy,especially with
Digitaltoolsand AI - Languages:Fluent in English;knowledge of Frenchisa distinctasset.
Offer:
- Being part of a company where innovation, collaboration, and impactaren'tjust values —they'rehow 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
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