Role Purpose:
1. An expert in Pipeline Link/Trial Link; updates databases with minimal supervision and is responsible for carrying out data aggregation around companys sales, financials, broker data as well as drug attributes
2. Carries out research and analysis of marketed and late-stage R&D products of pharmaceutical companies to cover information on clinical trial data and approval timelines
3. Own, manage and develop the database/analytics tool/dashboard, improve the capabilities of current databases and tools
4. Support analysts/editors in research and quantitative projects
Principal Accountabilities:
1. Gather and analyze information from multiple secondary sources for the purpose of writing R&D news and summaries for GMI clients.
2. Contribute to R&D Intelligence database, write clear and crisp summaries of latest pre-clinical/clinical developments (including phase changes, regulatory and licensing updates, presenting clinical data, and identifying M&A opportunities for clients).
3. Updating the databases with relevant updates such as clinical trial updates, regulatory updates, company predictions and clinical data.
4. Work on company pipelines and keep the database up to date with most recent changes in the pipelines.
5. Liaise with pharma/biotech companies to validate and compile latest updates in their respective R&D portfolio.
6. Coordinate with internal stakeholders on an ongoing basis and consistently deliver quality output.
7. Thoroughly comprehend the business rules and manage the products in the system according to the SOP.
8. Timely delivery of all the projects/activities
9. Managing processes independently
10. Actively drive and/or participate in existing product enhancement and process improvement initiatives, new product development ideas
Minimum Education, Experience, & Specialized Knowledge Required:
Education:
UG: Graduation in Life Sciences/Pharma-B.Pharma/Biotechnology and/or
PG: Masters degree in Pharmaceutical Sciences or Life Sciences
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