Role Purpose: 1. An expert in Pipeline Link/Trial Link; updates databases with minimal supervision and is responsible for carrying out data aggregation around company’s 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: Master’s degree in Pharmaceutical Sciences or Life Sciences * For experienced candidates, a post graduate degree or diploma is not essential. Experience: 1. 4-8 years of experience in pharmaceutical analytics 2. Experience in managing tasks/teams, timelines, and project management Skills: 1. Good understanding of preclinical and clinical scientific information 2. Good secondary research skills - advanced search options in Google and knowledge regarding various company reports (10K, 20F, press releases, investor presentations), clinical trial registries and regulatory agencies websites 3. Excellent writing skills 4. Good communication skills with ability to clearly, articulate the message without causing any confusion. 5. Proficient in MS Office (e.g., Word, Excel, PowerPoint). 6. Excellent secondary research skills and knowledge of various sources like regulatory agency websites, etc. 7. Pipeline creation, validation and clinical trial analysis 8. Good understanding of the commercial pharmaceutical market, major companies, latest trends, and therapy areas 9. Excellent project management skills (potential to work with multiple data sets at any given time) 10. Proficient in MS Office (e.g., Word, Excel, PowerPoint) 11. Good verbal and written communication skills 12. Knowledge and prior experience of IQVIA Health databases Additional Requirements: 1. Flexibility (should be ready to take additional responsibility whenever there is an increased work load or decreased capacity) 2. Attention to detail; Drive team for successful deliveries 3. Good communication skills (written and spoken English) with ability to clearly, articulate the message without causing any confusions 4. Good interpersonal skills (should have good listening skills, patience and handle situations in a calm and composed way) 5. Good team player/management skill (should be ready to share the work among the team members and helping the team meet the deadlines) 6. Strong team player and able to collaborate at all levels and across geography but also able to work under own initiative 7. Project management with the ability to perform under pressure. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled