Ph3Job Description Summary /h3 p#LI-Hybridbr/Location: Baselbr/This role is based in Basel, Switzerland. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. /p pWe are Clinical Sciences and Innovation at Novartis. A dynamic group of Clinical Trial Leaders (Clinical Scientists) who plan and execute early phase trials worldwide. From First-in-Human to ph2a studies and beyond. We design and operationalize trials, ensuring they run smoothly, on time and – most importantly – with patients’ interests to the fore. /p pCurious, unbossed and inspired; we are committed to flexibility in the workplace. /p pAs a member of our team, you will support or lead the clinical science and operations of planning and executing translational medicine clinical trials. Collaborate across our global network. Partner with outstanding physicians and scientists. Build therapeutic area expertise. Revolutionize next-generation, digital and patient‑centric trial design. Be always curious, innovative and inspiring. /p pThis position will be located at the Novartis Headquarter in Basel and will not have the ability to be located remotely. This position may require up to 5% travel time as defined by the business. /p h3Job Description /h3 h3Key Responsibilities /h3 ul liOperationally and scientifically lead complex clinical studies /li liDrive and deliver aspects of global clinical trial execution from study design, set‑up and recruitment to final reporting /li liLead the matrix‑management of robust global clinical trial teams, collaborating across the organization and externally with service providers/investigator sites /li liDrive the development of clinical study protocols, clinical operations execution plans and other required documents /li liEnsure quality conduct and document standards are applied across the clinical trial lifecycle /li liLead clinical data review (bSr. Clinical Sciences Trial Leader /b) /li liSupport clinical data review (bClinical Sciences Trial Leader /b) /li liContribute to project/program level plans (bSr. Clinical Sciences Trial Leader /b) /li liMay mentor junior team members /li liSupport optimization of standard methodologies in clinical trial operations and adopt an open learning and sharing environment /li liUnleash the value of data and digital within clinical studies Ultimately, YOU will help bring new technologies and therapies closer to our patients /li /ul h3Essential Requirements /h3 ul liA minimum of BSc in life sciences is required. A MSc, PharmD or PhD is desired. /li libClinical Sciences Trial Leader /b: 2‑4 years’ experience, in clinical trial management/operations, coupled with a broad knowledge of the drug development field; preferably within the pharma industry. /li libSr. Clinical Sciences Trial Leader /b 4+ years’ experience in clinical trial management/operations, coupled with a broad knowledge of the drug development field; preferably within the pharma industry. /li libClinical Sciences Trial Leader /b level: Leadership potential and well‑developed interpersonal skills. /li libSr. Clinical Sciences Trial Leader /b level: Demonstrated leadership experience and well‑developed interpersonal skills. /li liA track record of collaborating with and influencing a wide range of people, and of building strong partnerships /li liStrong project management experience; excellent planning, prioritization and organizational skills; used to managing multiple priorities concurrently /li liHigh change agility, thriving in an open and dynamic environment. /li liAble to learn proactively, tackle issues and take accountability /li liClear written and verbal expression of ideas; an active communicator /li /ul h3Desirable Requirements /h3 ul liExperience in study design and protocol development/writing is highly desirable /li /ul pThis is a dual posting. The final level title of the offer role would be determined by the hiring team based on the skills, experience capabilities required to perform the role at the level the role has been offered. /p h3Accessibility and accommodation /h3 pNovartis 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 in order to receive more detailed information about the essential functions of a position, please send an e‑mail to and let us know the nature of your request and your contact information. Please include the job requisition number in your message /p h3Skills Desired /h3 ul liAuditing /li liClinical Monitoring /li liClinical Research /li liClinical Study Reports /li liClinical Trial Management Systems /li liClinical Trials /li liData Auditing /li liData Management /li liHealth Sciences /li liLifesciences /li liProject Planning /li liVendor Management /li liWaterfall Model /li /ul /p #J-18808-Ljbffr