PpLocation: Basel, Switzerland. This role is based in Basel; no relocation support is offered. A maximum of 5% travel is required. /ph3Key Responsibilities /h3ulliOperationally and scientifically lead complex clinical studies /liliDrive and deliver aspects of global clinical trial execution from study design, set‑up and recruitment to final reporting /liliLead the matrix‑management of robust global clinical trial teams, collaborating across the organization and with external service providers and investigator sites /liliDrive the development of clinical study protocols, clinical operations execution plans and other required documents /liliEnsure quality conduct and document standards are applied across the clinical trial lifecycle /liliLead clinical data review (for Senior Clinical Sciences Trial Leaders) /liliSupport clinical data review (for Clinical Sciences Trial Leaders) /liliContribute to project/program level plans (for Senior Clinical Sciences Trial Leaders) /liliMay mentor junior team members /liliSupport optimization of standard methodologies in clinical trial operations and promote an open learning and sharing environment /liliUnleash the value of data and digital within clinical studies /liliBring new technologies and therapies closer to patients /li /ulh3Essential Requirements /h3ulliA minimum of a BSc in life sciences /liliA MSc, PharmD or PhD is desired /liliClinical Sciences Trial Leader: 2‑4 years’ experience in clinical trial management/operations, with broad knowledge of drug development, preferably within the pharma industry /liliSenior Clinical Sciences Trial Leader: 4+ years’ experience in clinical trial management/operations, with broad knowledge of drug development, preferably within the pharma industry /liliLeadership potential and well‑developed interpersonal skills (for Trial Leader level) /liliDemonstrated leadership experience and well‑developed interpersonal skills (for Senior level) /liliTrack record of collaborating with and influencing a wide range of people and building strong partnerships /liliStrong project management experience; excellent planning, prioritization and organizational skills; able to manage multiple priorities concurrently /liliHigh change agility, thriving in an open and dynamic environment /liliAbility to learn proactively, tackle issues and take accountability /liliClear written and verbal expression of ideas; an active communicator /li /ulh3Desirable Requirements /h3ulliExperience in study design and protocol development/writing /liliExperience with clinical monitoring, audits, data auditing, data management and clinical trial management systems /liliKnowledge of health sciences, life sciences, project planning, vendor management and waterfall model approaches /li /ulpAccessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or to receive more detailed information about the essential functions of a position, please email and provide the job requisition number. /p /p #J-18808-Ljbffr