GN Industry LS Clinical Consultant Accenture services Pvt Ltd

6.0 - 8.0 years

0 Lacs

bengaluru, karnataka, india

On-site

Job Title - Research & Development Consultant Life Sciences Management Level : 09,11 Location: Bangalore/ Gurgaon/Hyderabad/Mumbai Job Summary: MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire and analysis, operating model, business process mapping, and so on. Preferably worked with R&D functions such as Laboratory functio...

Posted 1 day ago

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Pharmacovigilance Systems Specialist ICON plc

0.0 years

0 Lacs

chennai, tamil nadu, india

On-site

Pharmacovigilance Systems Specialist ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Pharmacovigilance Systems Specialist to join our diverse and dynamic team. As a Pharmacovigilance Systems Specialist at ICON, you will be responsible for managing and optimizing pharmacovigilance databases and systems to ensure efficient data handling and compliance with regulatory requirements. Your technical expertise and attention to detail will be essential in supporting...

Posted 5 days ago

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SME - PCI IDS Infotech

7.0 - 12.0 years

6 - 10 Lacs

Chandigarh

Work from Office

Band : TBD Position Overview: Subject Matter Expert PCI Business We are seeking an experienced Subject Matter Expert (SME) in Pharmacovigilance Research to lead drug safety monitoring, regulatory compliance, and risk assessment initiatives. This role requires deep expertise in pharmacovigilance regulations, adverse event management, and clinical trial safety assessments. The SME will provide strategic guidance, ensure compliance with global regulatory standards, and support process optimization within pharmaceutical and biotech industries. Key Responsibilities Establish and maintain production and quality control protocols for data collection, analysis, and reporting processes Develop and im...

Posted 6 months ago

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