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Wipro Limited (NYSE: WIT, BSE: 507685, NSE: WIPRO) is a leading technology services and consulting company focused on building innovative solutions that address clients’ most complex digital transformation needs. Leveraging our holistic portfolio of capabilities in consulting, design, engineering, and operations, we help clients realize their boldest ambitions and build future-ready, sustainable businesses. With nearly 245,000 employees and business partners across 65 countries, we deliver on the promise of helping our clients, colleagues, and communities thrive in an ever-changing world.
- Vacancy details:
- Post Name: Drug safety analyst – Literature specialist
- Qualification: PhD / Pharm D / M.Pharm / B.Pharm / BDS / B. Tech/M.Tech.(Lifesciences), M.Sc./B.Sc. (Lifescience)
- Experienced: 4+ yrs experience in Pharmacovigilance experience. Required understating of bibliographic database & search libraries (at least 1 year hands on experience in crafting & executing search strategies)
Job Description: Greetings from Wipro Technologies pvt ltd .!!
Important Details :
- Location: Pune, Maharashtra, India
- Post of date:05/12/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Wipro is Hiring for Drug safety analyst – Literature specialist (Pune Location)!!!
Experience:
4+ yrs experience in Pharmacovigilance experience. Required understating of bibliographic database & search libraries (at least 1 year hands on experience in crafting & executing search strategies)
Should know to construct strings on the database-MUST
Education Qualification:
PhD / Pharm D / M.Pharm / B.Pharm / BDS / B. Tech/M.Tech.(Lifesciences), M.Sc./B.Sc. (Lifescience)
Role & Responsibility
1. Oversee the execution & implementation of data acquisition and data management processes that support Pharmacovigilance activities
2. Construct & execute optimally search strategies on biomedical database & content aggregators platforms
3. In-Depth knowledge about pharmaceutical industry, product terminology, drug nomenclature, drug class hierarchies
4. Understanding about medical terminologies and search syntax for leadings search databases / platforms i.e. OVID, Embase, Medline, Pubmed, etc.
5. Ability to perform comprehensive review of literature and analysis of scientific published literature to support health agency requests, product submissions.
6. Maintain awareness and understanding of relevant technologies that could support improvements in content acquisition.
7. Oversee and interact with external vendors (i.e. content partners)
8. Liaison with inter & intra team to meet the end to end process needs and meet business objectives
9. Innovative mindset to drive efficiencies and develop solutions that meet process & customer needs
10. Demonstrate High learning agility to learn and implement the latest tools/technologies
Salient Required / Essential Skills
• Knowledge about bibliographic dataset and content libraries
• Hands on experience in setting-up searches on OVID / EMBASE / MEDLINE
• Proven scientific literature searching skills with experience applying pharmaceutical databases and resources
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