Development jobs

Summary #LI-Onsite Location: HYD, India This role is based in Hyderabad, India. Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for you.

Summary We are seeking an experienced Technical Operations Lead with Pharmaceutical domain expertise and knowledge of R/Python programming/latest technology platforms to support a global pharmaceutical Operations engagement.

Summary The Head of Medical Safety Assessment and External Engagement within Medical Safety Operations, is responsible overseeing the quality of medical review of safety cases in the Novartis Safety system including External Service Providers (ESP).

Summary As a Materials Science Project Lead, you will provide scientific and project leadership for Active Pharmaceutical Ingredient (API) crystallization and finishing process-development activities, as well as solid-form activities performed at strategic external partners in India.

Summary As part of the ARD Data & Digital organization, the Associate Director – Validation Lead, Data & Digital is accountable for leading TRD’s digital capability validation strategy execution and governance, ensuring systems are implemented/deployed with the highest standards of compliance.

Summary -Responsible and accountable for managing all Data Mgmt/Coding / CDD/DAP aspects of several studies, a medium to large sized project or project level activities at a consistently high standard.

Summary Role Type: Hybrid Working, #LI-Hybrid Location: Hyderabad, India Relocation Support: Yes What if your expertise could help turn complex radioligand therapy data into reliable insights for oncology development?

Summary Role Type: Hybrid Working, #LI-Hybrid Primary Location: Hyderabad, India Other Location: Mumbai, India Relocation Support: Yes What if your technical leadership could transform how clinical trial risks are detected and managed?

Summary -Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures within a multifunctional project team coordinated by a Project Leader. Manage technical lab/plant activities.

Summary The Principal Data Scientist is responsible and accountable for managing all Data Management activities using advanced data management tool and techniques with respect to cost, quality and timelines for all assigned projects/trials within a Clinical Program.

Summary Responsible for managing regulatory clinical trials or maintenance activities independently. The GRM focuses on the delivery of regulatory activities related to clinical trial applications or to the maintenance of the assigned portfolio for selected countries/region.

Summary -Responsible and accountable for managing all Data Mgmt/Coding / CDD/DAP aspects of several studies, a medium to large sized project or project level activities at a consistently high standard.

Summary The Expert Clinical Data Scientist is responsible and accountable for using advanced data management tools and techniques with respect to cost, quality and timelines for all assigned trials managed within Clinical Data Acquisition and Management.

Summary Responsible and accountable for managing all Data Mgmt/Coding / CDD/DAP aspects of several studies, a medium to large sized project or project level activities at a consistently high standard.

Summary -Contributes, with appropriate oversight, to all relevant aspects of global clinical trial(s) activities to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial Team.

Summary Provide expertise and cross functional leadership on pharmacovigilance and/or device vigilance for all assigned Novartis Enterprise contractual arrangements including Global and Local Vigilance Agreements, and Clinical Trial Supply Agreements; and the management of transition of vigilance systems and processes

Summary -Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures within a multifunctional project team coordinated by a Project Leader. Manage technical lab/plant activities.