As a Senior Clinical Sciences Trial Leader, you will lead the clinical science and operations of planning and executing translational medicine clinical trials. Collaborate across our global network and partner with outstanding physicians and scientists. By building your therapeutic area expertise, you will deliver next-generation, digital and patient-centric trial designs. Being always curious, innovative and inspiring.

More specifically, you will:
• Operationally and scientifically lead complex clinical studies.
• Drive and deliver aspects of global clinical trial execution from study design, set-up and recruitment to final reporting.
• Lead the matrix-management of robust global clinical trial teams, collaborating across the organization and externally with service providers/investigator sites.
• Drive the development of clinical study protocols, clinical operations execution plans and other required documents.
• Ensure quality conduct and document standards are applied across the clinical trial lifecycle.
• Lead or support clinical data review
• Contribute to project/program level plans

• May mentor junior team members as required.
• Support optimization of standard methodologies in clinical trial operations and adopt an open learning and sharing environment.
• Unleash the value of data and digital within clinical studies.

Ultimately, YOU will help bring new technologies and therapies closer to our patients.

Minimum requirements :

• In this role, you will bring:
  • A life sciences PhD or PharmD (desirable), or BSc or MSc in life sciences.
  • 4+ years’ experience in clinical trial management/operations, coupled with a broad knowledge of the drug development field; preferably within the pharma industry.
• Demonstrated leadership experience and well-developed interpersonal skills.
• A track record of collaborating with and influencing a wide range of people, and of building strong partnerships, inspiring mutual respect and fostering a positive, inclusive team culture.
• Strong project management experience; excellent planning, prioritization and organizational skills; used to managing multiple priorities concurrently.
• Strong scientific and clinical expertise with the ability to interpret and represent trial-level data, while maintaining a patient-centric mindset that integrates patient insights into protocol development, trial planning, and execution.
• High change agility, thriving in an open and dynamic environment. Able to learn proactively, tackle issues and take accountability.
• Clear written and verbal expression of ideas; an active communicator.

Final job title and associated responsibilities will be commensurate with the successful candidates’ level of expertise.

Why Novartis? Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards 

Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network