P2518 - Senior Clinical Data Manager (Early Phases)

We are currently looking for a motivated and collaborative professional to join our Data Management and Biostatistical department based at our Headquarters in Lausanne, Switzerland asSenior Clinical Data Manager - early phases As a Senior Clinical Data Manager, you won't just manage data; you will be the data strategy leader for assigned clinical studies, pioneering innovative approaches to data flow, quality, and accessibility. You are accountable for ensuring the timely availability of complete, accurate, and consistent clinical data to support critical and rapid internal decision-making, particularly in our early-phase and adaptive trials.You will act as the key liaison between the technology and clinical functions, leveraging your expertise in modern data capture and cleaning tools to support smart, efficient clinical development.Your Mission. Innovation & Data Strategy: Pioneer Data Integration: Drive the strategy for integrating complex data sources (e.g., ePRO, wearables, central lab, biomarker data) into the Electronic Data Capture (EDC) system and clinical database for unified, streamlined analysisAgile Data Management: Define and manage timelines for multiple clinical studies or development programs, applying agile data management principles to support the fast-paced, adaptive needs of early-phase clinical developmentSmart Cleaning & Validation: Oversee and/or perform the setup of sophisticated EDC systems and data validation plans, implementing risk-based and automated data quality checks to focus manual review efforts on the most critical data pointsTechnology Leadership: Act as a key technical reference for transversal activities, coordinating the evaluation and implementation of new data management tools and technologies to enhance efficiency and quality across the departmentOversight, Quality & ComplianceEnd-to-End Oversight: Prepare, review, and ensure execution of comprehensive Oversight Plans and Data Management Plans (DMPs), maintaining accountability for all outsourced and in-house data management activitiesEDC & Database Mastery: Lead the full lifecycle of the clinical database, including complex Electronic Case Report Form (eCRF) design, User Acceptance Testing (UAT), database release, and final lock/transfer/archive, ensuring the system supports evolving study protocolsData Integrity Champion: Ensure ongoing and timely data capture, cleaning, and reconciliation activities. Champion data quality according to industry standards and strict data integrity principles (ALCOA+)Ensure that all data management activities are fully compliant with GCP, applicable regulatory guidelines, and company Procedural DocumentsMore than a checklist of skills, we're looking for someone who shares our commitment to science with purpose.RequirementsMaster in Life Sciences or similar educationAt least 8+ years of progressive experience in Clinical Data Management at Sponsor Pharmaceutical & Biotech Proven experience as the lead Data Manager overseeing the end-to-end data management strategy for an entire development programs, particularly those supporting complex or adaptive trial designs·Strong, hands-on experience utilizing and optimizing several industry-leading EDC systems (e.g., Rave, InForm) and related data management and cleaning technologiesExperience managing data for early-phase (Phase I/II) studies is a significant advantage, demonstrating an ability to rapidly adjust to protocol changes and expedited timelinesExceptional planning, organizational, and communication skills essential for managing multiple parallel study timelinesAbility to effectively work and collaborate as a key member of the clinical study team within a complex matrix organizationFluent in English; good knowledge of French is an assetTeam oriented, you look for a collaborative workspace where your can share & learn with and from your colleaguesWhat to Expect in the Recruitment Process:If 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.Please contact our HR Department prior to submitting any profiles. We cannot accept unsolicited applications from agencies or recruiters.BenefitsBeing part of a company where innovation, collaboration, and impact aren't just values — they're how we work every dayPartner with teams across disciplines, at the forefront of oncology and anti-infective developmentAn inclusive and respectful workplace — proud to be Equal-Pay certifiedGrow in a culture that values people, purpose, and performanceA chance to grow, share, and shape the future of healthcare