P2617 - Senior Clinical Data Manager

ph3Together, we innovate, we impact, we grow /h3 pAtDebiopharm, 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 are driven by science, but above all, by the people behind every treatment – the patients and their families. /p pThrough 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 /h3 pPermanent 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 ul libStudy Leadership: /b Lead and coordinate CDM activities, including CRF design, EDC system set‑up, User Acceptance Testing (UAT), and database release. /li libOperational Excellence: /b Perform data review, query generation, and data coding while ensuring timely data capture from both internal and external sources. /li libStrategic Planning: /b Define and manage timelines for multiple studies or development programmes. /li libDocumentation Compliance: /b Prepare and review Data Management Plans (DMP) and validation plans in strict compliance with GCP, SOPs, and regulatory guidelines. /li libLifecycle Management: /b Oversee the lock, transfer, and archiving of clinical study databases. /li libCollaboration: /b Act as a key member of the clinical study team, working closely with Clinical Trial Managers and other stakeholders in a matrix environment. /li /ul h3Your Profile /h3 ul libEducation: /b Scientific or technical background, ideally at a university level. In addition, any Project Management certification would be a plus. /li libExperience: /b At least 10 years in clinical data management, working in a 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 libTechnical Expertise: /b Strong experience with various EDC systems and first experience or proficiency automating activities with AI. /li libLeadership: /b Proven track record in leading data management studies and teams to deliver high‑quality, regulatory‑compliant databases. /li libSkills: /b Excellent organisational, planning/coordination, proactivity and communication skills. Tech‑savvy, especially with Digital tools and AI. /li libLanguages: /b Fluent in English; knowledge of French is a distinct asset. /li /ul h3What we Offer /h3 ul liBeing part of a company where innovation, collaboration, and impact aren’t just values – they’re how we work every day. /li liPartner with teams across disciplines, at the forefront of oncology and anti‑infective development. /li liAn inclusive and respectful workplace – proud to be Equal‑Pay certified. /li liGrow in a culture that values people, purpose, and performance. /li liA chance to grow, share, and shape the future of healthcare. /li /ul /p #J-18808-Ljbffr