About the Role
Clinical Project Manager
Location – Hyderabad #LI Hybrid
About the Role:
This role is responsible to Lead and... ...evaluation and implementation of assigned clinical studies and/or MAP//Research Collaborations/IIT/Digital Solutions programs according to...
...of the LCTL/CTL, as assigned. Support the clinical protocol development process in... ...and internal/external presentations.
coordinate the real time availability of quality clinical... ...Management Department as well as with the Assay Research Lab. This also includes the set-up,...
...TM), in Novartis Institutes of Biomedical Research (NIBR). It is an enterprise organization,... ..., pharmacodynamics, metabolism and clinical pharmacology in advancing the drug candidates... ...support of clinical trials for biologics . Coordinate and monitor PK, PD, anti-drug (ADA) and...
...collected and in alignment with the protocol.
• Support the assessment of new data collection requirements in assigned studies and provide clinical input into the development of new and updated clinical Data Standards (for CRFs as well as 3rd party data collection methodologies)...
...About the role
“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical... ...).
•
1 year experience in pharmaceutical industry/ clinical research organization - Basic knowledge in planning, executing, reporting...
...the Role
Job Purpose
The Head of Operational Excellence, Clinical Development will be accountable for leading key strategic global... ...strategy aligned with the organization’s goals.
• Coordinate in partnership with Talent, Capability and Communications partners...
...Independently manage and execute drug shipment ticket review process (US)
• In addition to regulatory manager, provide guidance to clinical functions on regulatory compliance activities, such as requirements for TOOs, VDRs, drug shipment etc.
• Assist regulatory managers...
...About the role
Clinical Data Scientist
Location – Hyderabad/ Mumbai
About the Role:
Provide timely and professional ongoing management of Data Management deliverables and of clinical trial data with respect to cost, quality and timelines for all assigned trials...
...About the role
Principal RWE Research Analyst
Location – Hyderabad #LI Hybrid
About the Role:
The Principal Real World Evidence... ...in a closely related field within the pharma industry (e.g., clinical research, statistics, epidemiology, pricing).
• Master’s degree...
About the Role
Your responsibilities will include, but are not limited to:
• Represents GCS as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT on the optimal clinical trial supply strategy in terms of, but not limited to, packaging...
...About the role
Manager – Primary Market Research
Location – Hyderabad #LI Hybrid
About the Role:
Be part of a leading healthcare primary market research team working with brand teams across the globe, as part of Novartis’ longer term strategic plan, to bring a new...
...Responsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA)... ...equivalent with ≥ 2 years’ experience in Clinical research with proven proficiency in global Clinical development...
...role
2025! This is the year that Global Clinical supply is targeting for completing the... ...and be a key interface between Technical Research & Development (TRD) teams and the... ...term demand and capacity planning (LTDCP) coordinating with the CSPL, DPPL, DSPL and TPL.
• Adheres...
...and/or improvements.
The MS P&P Lead supports planning and coordination of daily operational activities to ensure process... ...setting, preferably in drug safety (i.e., Pharmacovigilance), clinical research, or regulatory affairs (incl. appropriate business case development...
...Engineer
Location: Hyderabad
Novartis Institutes for BioMedical Research (NIBR) is the global pharmaceutical research organization of... ..., visualization, and interpretation of chemical, biological, clinical and operational data.
Key Responsibilities:
• Develop state...
...is responsible to design and execute data management strategy across Drug Development line functions i.e. Clinical Operations, Clinical Data Standards, Technical Research & Development, Regulatory Affairs and Patient Safety. Function also collaborates with cross domains such...
...listings and figures for Interventional and Non-Interventional Clinical studies.
Maintain efficient interfaces with other statisticians... ...of/experience with SAS/ R/ Splus or any other business or research analytic software with an expertise in at least one software....
...to:
• Provides scientific and medical expertise on assigned clinical projects. Contributes to clinical strategy for the Asian region... ...trial data medical/scientific review for assigned TCO projects and coordinates data analysis and interpretation including the development of...
...contributor in driving the #GO-Digital vision of Novartis.
Key Responsibilities:
• Lead and coordinate activities of all statistical programmers as Trial Programmer for phase I to IV clinical studies or assigned project-level activities. Make statistical programming...
...partner with global stakeholders to provide competitive intelligence research and analysis.
Your Key Responsibilities:
• Provide inputs through secondary data research and creating summaries for clinical and business events (periodic newsletter, news alerts)
• Provide...
...critical business problems. Understand life science data sources including preclinical, clinical, sales, contracting, promotions, social media, patient claims and Real-World Evidence
• Research and co-develop with supervisor in data management, new algorithms, methods,...
...Leader is responsible for the execution and delivery of the Global Clinical Operations (GCO), clinical studies in accordance with the... ...equivalent). 12- 15 years of Industrial experience in Clinical Research or Drug Development in any Phase.
• Significant recent experience...
...scientific/technical studies. By bridging the analytical science to the clinical performance you will drive the transformation of our molecules... ...is based in the Genome Valley, Hyderabad, within the Technical Research and Development Organization (TRD) of Global Drug Development (...
...and Licensing (BD&L) groups, medical contribution to the overall clinical strategy and individual clinical studies in close collaboration... ...functions e.g. patient safety.
• Identifies and engages with contract research organizations for selected GMD activities; supports Head Global...
...Millions! Novartis made a decision to pursue early discovery research internally to allow us to quickly translate the most impactful discoveries... ...Data Management team to enable reconciliation for locking of Clinical database. Alert the Medical Safety Physicians of potential...
...- Exercise Knowledge and Experience in Regulatory Agency Rules and Inspection Protocol as Well as Clinical Chemistry Best Practices to Enable the Most Advanced Research Capabilities Possible in the Laboratory
- Isolate, Analyze and Conduct Diverse Experiments with Proteins...
...Your responsibilities include, but are not limited to:
• Coordinate cross-divisional qualification, monitoring and governance activities... ...finalization/action completion in the Third-Party Management, Clinical Trial Quality Risk Management, and Supplier Lifecycle Management...
...content, including risk description and additional risk details. Coordinating with the Training lead to create and administer training and... ...along with project team members effectively.
• Knowledge of Clinical Trial Operations and Business Processes. Experience on BPMN 2.0...
...Translational Medicine (TM), in Novartis Institutes of Biomedical Research (NIBR). It is an enterprise organization, unique within... ...knowledge of pharmacokinetics, pharmacodynamics, metabolism and clinical pharmacology in advancing the drug candidates from discovery and...
...o Broad understanding of drug development – Early development, clinical trials, safety, data management, etc.
• Ability to lead the development... ...of big data capabilities and utilization as well as the coordination of cross-functional analytic initiatives.
• Work with...