Bangalore

11 July 2026

Apply Online for Quality Specialist at Teva

Compilation of high quality Annual Product Reviews / Product Quality Reviews for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and system

10 July 2026

Work as PV Case Processing Associate Manager at Elanco

Comply with internal and external timelines for managing adverse events and product complaint case processing, and case submission processes as appropriate.

10 July 2026

Work as Pharmacovigilance Services Specialist at Accenture

In this role you are required to do analysis and solving of moderately complex problems

5 July 2026

ICON plc Hiring Senior CDC

Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures. Manage clinical and third-party data reconciliation based on edit specifications and data review plans. ICON plc

2 July 2026

CDM Manager Post at Fortrea - Life Science / Pharmacy apply

B.Sc. degree in Life Science/Pharmacy or equivalent/related discipline or certification in a related allied health profession from an appropriately accredited institution

1 July 2026

Pharmacy graduates apply now for ICMR GMA Project at St. John's Research Institute

BSC (nursing) in experience in Pediatrics/ OBG, GNM, BSc/ Bcom/ B pharm /BE Familiarity with smartphones and data file management. Willing to work in chitradurga district.

1 July 2026

Require Associate Clinical Data Manager at Fortrea - Work from Home Job

University / college degree in life sciences, health sciences, information technology or related subjects preferred.

1 July 2026

Fortrea Hiring Regulatory Affairs Manager - Jobs in Bangalore, Mumbai, Pune, Remote India

Collaborate with peers across the organization to achieve client-centric delivery in a matrix organization. Collaboration across all stakeholders within Site Readiness

1 July 2026

PAREXEL Require Regulatory Affairs Associate

This role focuses on managing post-approval regulatory activities, including variations, renewals, and compliance with country-specific requirements. You will partner with cross-functional teams to ensure timely submissions and maintain regulatory dossiers.

29 June 2026

PAREXEL Hiring Senior Regulatory Affairs Consultant

Contribute to preparation and delivery of regulatory submissions from a global and regional perspective. Preparation and review of Marketing Authorization Applications & Variations for filing in US, EU, Japan, Canada Switzerland, Australia.

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