Drug Safety Analyst - Literature Specialist

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.