Wipro Pharmacovigilance Vacancies – Drug Safety Analyst | Pune

Wipro Pharmacovigilance Vacancies – Drug Safety Analyst

Are you passionate about ensuring drug safety and contributing to public health? Wipro, a global leader in technology and consulting services, is looking for a highly skilled Drug Safety Analyst – Literature Specialist to join their team in Pune, Maharashtra. This role is ideal for candidates with a strong background in pharmacovigilance and scientific literature review.

Job Description

Wipro is hiring experienced professionals for the position of Drug Safety Analyst – Literature Specialist in Pune. This role involves overseeing the execution and implementation of data acquisition and data management processes that support pharmacovigilance activities.

Responsibilities

As a Drug Safety Analyst at Wipro, you will:

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

Qualifications

To be considered for this role, you must have:

• Educational Background: PhD, Pharm D, M.Pharm, B.Pharm, BDS, B.Tech, M.Tech (Lifesciences), M.Sc, or B.Sc (Lifesciences).
• Experience: A minimum of 4 years of experience in pharmacovigilance, with at least 1 year of hands-on experience in bibliographic database searching and crafting search strategies.
• Skills:
  • Proficiency in setting up searches on OVID, EMBASE, MEDLINE.
  • Proven scientific literature searching skills.
  • Strong understanding of medical terminologies and search syntax for leading databases/platforms such as OVID, Embase, Medline, and Pubmed.

Key Skills

• Knowledge of bibliographic datasets and content libraries.
• Hands-on experience with OVID, EMBASE, and MEDLINE.
• Scientific literature searching expertise.
• Ability to perform thorough literature reviews and analyses.
• Strong communication and collaboration skills.

Application Process

Interested candidates can apply for this position on LinkedIn: Apply on LinkedIn

Tagged as: Good Clinical Practice (GCP)