7.0 - 9.0 years

0 Lacs

bengaluru, karnataka, india

On-site

Job Description Do you want to be part of an inclusive team that works to develop innovative therapies for patients Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. ?If you want to be part of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people througho...

Posted 1 month ago

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Central Monitoring Lead Astellas Pharma

5.0 - 9.0 years

0 Lacs

karnataka

On-site

Role Overview: You will be joining Astellas Pharma Inc., a global pharmaceutical company committed to developing innovative therapies for patients worldwide. As a Central Monitor at Astellas Global Capability Centres, you will play a crucial role in supporting drug development projects and ensuring the implementation of Risk Based Quality Management (RBQM) strategies. Your responsibilities will include collaborating with cross-functional study teams, conducting central monitoring activities, and overseeing the documentation and resolution of findings. Your expertise and leadership will contribute to the success of clinical trials and the advancement of medical solutions for patients. Key Res...

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Statistical Monitor Novo Nordisk

2.0 - 6.0 years

0 Lacs

karnataka

On-site

As a Statistical Monitor at Novo Nordisk Global Business Services (GBS) India, you will play a crucial role in supporting Risk-Based Monitoring within Clinical Drug Development by operating and maintaining the centralized Statistical Monitoring function. Your responsibilities will include analyzing clinical data across trials and projects to detect unusual data patterns, systematic errors, and potential instances of non-compliance or fraud that may not be identified through routine monitoring processes. By safeguarding data integrity, you will contribute significantly to the approval of new drugs. You will work closely with trial and project teams, as well as data management and programming ...

Posted 3 months ago

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