P2617 - senior clinical data manager

H3Together, we innovate, we impact, we grow /h3pAt 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.  /ppThrough our unique “development only” model, we bring forward promising therapies and transform them into treatments that can reach those who need them most, faster.  /p pAre you passionate about advancing science and improving lives? We are currently looking for a driven, passionate and collaborative professional to join our Biostatistics and Data Management department based at our Headquarters in Lausanne, Switzerland as  /p h3Senior Clinical Data Manager  /h3pPermanent role | Location: Lausanne, Switzerland  /p h3Your Mission  /h3 pAs a Senior 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.  /p h3Key Responsibilities  /h3 ullistrongStudy Leadership:  /strongLead and coordinate CDM activities, including eCRF design, EDC system setup, User Acceptance Testing (UAT), and database release.   /li /ulullistrongOperational Excellence:  /strongPerform data review, query generation, and data coding while ensuring timely data capture from both internal and external sources.   /li /ulullistrongStrategic Planning: /strong Define and manage timelines for multiple studies or development programs.   /li /ulullistrongDocumentation  Compliance: /strong Prepare and review Data Management Plans (DMP) and validation plans in strict compliance with GCP, SOPs, and regulatory guidelines.   /li /ulullistrongLifecycle Management:  /strongOversee the lock, transfer, and archiving of clinical study databases.   /li /ulullistrongCollaboration:  /strongAct as a key member of the clinical study team, working closely with Clinical Trial Managers and other stakeholders in a matrix environment.  /li /ul pstrongRequirements /strong /ph3Your profile  /h3 ullistrongEducation:  /strongScientific or technical background, ideally at a university level. In addition, any Project Management certification would be a plus.  /li /ulullistrongExperience:  /strongAt 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.  /li /ulullistrongTechnical Expertise: /strong Strong experience with various EDC systems and   first experience or proficiency automating activities with AI.   /li /ulullistrongLeadership:  /strongProven track record in leading data management studies and teams to deliver high-quality, regulatory-compliant databases.    /li /ulullistrongSkills:  /strongExcellent organizational, planning/coordination, proactivity and communication skills. Tech savvy, especially with Digital tools and AI  /li /ulullistrongLanguages:  /strongFluent in English; knowledge of French is a distinct asset.  /li /ulpstrongBenefits /strong /ph3What we Offer:  /h3 ulliBeing part of a company where innovation, collaboration, and impact aren’t just values — they’re how we work every day  /li /ululliPartner with teams across disciplines, at the forefront of oncology and anti-infective development  /li /ululliAn inclusive and respectful workplace — proud to be Equal-Pay certified  /li /ululliGrow in a culture that values people, purpose, and performance  /li /ululliA chance to grow, share, and shape the future of healthcare  /li /ul h3What to Expect in the Recruitment Process:  /h3 pIf your application is selected, you’ll be invited to interviews with Talent Acquisition and the Hiring Manager via Teams, followed by a panel interview and reference checks. Communication is handled via Workable—check your spam folder for emails from *@outbound.workable.com.  /p pPlease contact our HR Department prior to submitting any profiles. We cannot accept unsolicited applications from agencies or recruiters.  /p