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3.0 - 5.0 years
0 Lacs
hyderabad, telangana, india
On-site
Summary Location: Hyderabad, India At Novartis, we're reimagining medicine through data-driven insights and as an Evidence Generation Manager, you'll be at the heart of that transformation. In this role, you'll lead the development of innovative, non-interventional studies using real-world data to shape how our medicines are accessed and adopted globally. Your scientific leadership will empower regulators, payers, clinicians, and patients to make informed decisions, ultimately improving lives. If you're passionate about evidence strategy, thrive in a collaborative environment, and want to make a meaningful impact, this is your opportunity to do work that matters. About The Role Key Responsib...
Posted 1 week ago
3.0 - 6.0 years
3 - 6 Lacs
bengaluru, karnataka, india
On-site
Lead design and execution of RWE studies in close collaboration with internal stakeholders from Clinical Strategy, Medical Affairs, and Clinical Data Science. Author and/or oversee development of study protocols, reports, conference abstracts, and peer-reviewed publications using RWD and collaborate cross-functionally to integrate RWD into global publication strategies Ensure scientific rigor and serve as a methodology expert for real-world evidence generation; select and implement appropriate analytic methods aligned to research needs Collaborate closely with data management and biostatistics functions to ensure data quality and deliver robust data analyses utilizing scientifically valid an...
Posted 1 week ago
6.0 - 8.0 years
6 - 8 Lacs
hyderabad, telangana, india
On-site
Lead and develop technical programming and process improvement initiatives within CfOR Design data quality enhancements Represent the programming function and participate in multidisciplinary project team meetings Project manage all programming activities, according to agreed resource and timeline plans Ensure all programming activities on the project adhere to departmental standards Write and/or review and approve all programming plans Write and/or review and approve analysis dataset specifications Review and approve key study-related documents produced by other functions, e.g. SAPs, CRF, Data Management Plan, etc. Write, test and validate software programs in Unix to produce analysis datas...
Posted 2 months ago
6.0 - 10.0 years
6 - 10 Lacs
Pune, Maharashtra, India
On-site
The Senior Specialist, Global Commercial Pharma Pipeline Analytics, HHDDA will be responsible for developing and delivering data and analytics, generating strategic insights, and addressing global brand lead's business questions to inform pharma pipeline investments and beyond G7 investments. Furthermore, the team member will partner closely with global marketing, regional marketing, clinical and discovery, finance & enterprise strategy teams to inform executive decision making through analytics support for clinical development, business development and alliances/partnerships decisions. The team member will partner closely with our pipeline forecasting capabilities by leveraging real world, ...
Posted 3 months ago
6.0 - 8.0 years
6 - 8 Lacs
Hyderabad / Secunderabad, Telangana, Telangana, India
On-site
What you will do Lets do this. Lets change the world. In this vital role you will Provide technical solutions to programming problems within CfOR Lead and develop technical programming and process improvement initiatives within CfOR Design data quality enhancements Represent the programming function and participate in multidisciplinary project team meetings Project manage all programming activities, according to agreed resource and timeline plans Ensure all programming activities on the project adhere to departmental standards Write and/or review and approve all programming plans Write and/or review and approve analysis dataset specifications Review and approve key study-related documents pr...
Posted 5 months ago
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