4 Global Regulatory Jobs

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7.0 - 11.0 years

0 Lacs

hyderabad, telangana

On-site

As the Evidence Generation Director at Novartis, you will play a crucial role in contributing to the product medical strategy and integrated evidence planning. Your expertise will be instrumental in leading cross-functional teams to develop and execute innovative evidence strategies. Your responsibilities will encompass a wide range of scientific, technical, and strategic aspects to ensure the successful delivery of impactful evidence solutions. **Key Responsibilities:** - Provide scientific oversight and leadership for various study types, including interventional and non-interventional studies, consistent with Integrated Evidence Plans (IEP). - Develop study concepts, protocols, and report...

Posted 3 weeks ago

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5.0 - 9.0 years

0 Lacs

chennai, tamil nadu

On-site

Role Overview: As a Sec & Derivatives Sr Analyst at our company, you will be responsible for processing orders and transactions originating from trading desks and branch offices. Your main objective will be to facilitate the clearance, settlement, and investigation of client securities and derivatives transactions. Key Responsibilities: - Experience in non-financial regulatory and tax reporting (SME) - Demonstrate an excellent understanding of OTC derivatives and investment products - Possess excellent spoken and written English skills - Showcase excellent presentation and communication skills, with the ability to adjust communication style to the recipient - Understand operational risks and...

Posted 1 month ago

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2 - 6 years

7 - 10 Lacs

Hyderabad, Bangalore Rural, Mumbai (All Areas)

Work from Office

Hi We are hiring for Regulatory Submissions Publisher . Job Purpose: Build and process submission dossiers of low-to-moderate complexity: Submission Dossiers that may be periodic (e.g.: safety reports) or minor amendments (e.g.: IND Amendment, DMF Amendment, CMC Update as appropriate to level, etc) or otherwise not major applications but in support of pending approvals or lifecycle commitments for marketed products (e.g.: meeting packages, responses as appropriate, Advertising and Promotion Submissions, routine labeling updates as appropriate, etc.) QC submission dossiers or parts of submission dossier output of low-to-moderate and moderate-to-high complexities as assigned. Other submission ...

Posted 5 months ago

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2 - 5 years

6 - 10 Lacs

Noida

Work from Office

Hi, We are hiring for leading ITES Company for Narrative Medical Writing Profile . Job Description Build and process submission dossiers of low-to-moderate complexity: Submission Dossiers that may be periodic (e.g.: safety reports) or minor amendments (e.g.: IND Amendment, DMF Amendment, CMC Update as appropriate to level, etc) or otherwise not major applications but in support of pending approvals or lifecycle commitments for marketed products (e.g.: meeting packages, responses as appropriate, Advertising and Promotion Submissions, routine labeling updates as appropriate, etc.). QC submission dossiers or parts of submission dossier output of low-to- moderate and moderate-to-high complexitie...

Posted 5 months ago

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