Are you passionate about pharmacovigilance and scientific literature analysis? Wipro, a global leader in technology and consulting services, is currently hiring for the position of Drug Safety Analyst – Literature Specialist in Pune. This role offers a unique opportunity to contribute to the healthcare and pharmaceutical industry through your expertise in literature review, database search strategies, and pharmacovigilance processes.
Company Introduction: About Wipro
Wipro Limited is a leading global IT, consulting, and business process services company. With over 200,000 employees worldwide, Wipro has a strong presence in more than 50 countries. It offers a diverse range of services in IT, healthcare, and life sciences, providing innovative solutions that drive business transformation. Wipro’s Life Sciences division works closely with global pharmaceutical and healthcare companies to support their clinical research, regulatory compliance, and pharmacovigilance efforts.
Responsibilities in the Job
As a Drug Safety Analyst – Literature Specialist, your primary responsibilities will include:
- Pharmacovigilance Data Management: Oversee the execution of data acquisition and management processes for pharmacovigilance activities.
- Search Strategy Construction: Build and execute efficient search strategies on biomedical databases and content aggregator platforms.
- Comprehensive Literature Review: Perform in-depth analysis and reviews of scientific publications to support regulatory submissions and health agency requests.
- Content Acquisition: Stay updated on relevant technologies to improve content acquisition processes.
- Team Collaboration: Liaison with internal and external teams, including vendors, to meet business objectives and ensure process efficiency.
- Innovation & Efficiency: Drive innovative solutions to streamline processes and improve outcomes in literature searches and pharmacovigilance activities.
Qualifications
To be eligible for this role, you should have:
- Educational Background: PhD, Pharm D, M.Pharm, B.Pharm, BDS, B.Tech/M.Tech (Life Sciences), M.Sc. or B.Sc. in Life Sciences.
- Experience: A minimum of 4 years of experience in pharmacovigilance, with at least 1 year of hands-on experience in bibliographic databases and search libraries like OVID, Embase, Medline, and PubMed.
Skills
The ideal candidate should possess:
- Pharmacovigilance Expertise: Strong knowledge of the pharmaceutical industry, drug nomenclature, product terminology, and drug class hierarchies.
- Bibliographic Database Proficiency: Experience in constructing and executing search strategies on OVID, Embase, Medline, PubMed, and other leading search platforms.
- Scientific Literature Analysis: Proven ability to review and analyze scientific publications to support regulatory needs.
- Innovative Mindset: A keen interest in driving efficiencies and adopting the latest technologies and methodologies.
- Team Collaboration: Strong interpersonal skills to work effectively with cross-functional teams and external vendors.
