Wipro Hiring: Drug Safety Analyst – Literature Specialist in Pharmacovigilance at Pune
Position Name:
Drug Safety Analyst – Literature Specialist
Organization:
Wipro
Qualification:
PhD / Pharm D / M.Pharm / B.Pharm / BDS / B. Tech / M.Tech (Life Sciences), M.Sc. / B.Sc. (Life Sciences)
Experience:
4+ years of experience in pharmacovigilance
Salary Range:
INR 5,80,000 – INR 10,00,000
Location:
Pune
About Wipro
Wipro Limited is a leading global IT, consulting, and business process services company with over 200,000 employees in more than 50 countries. Renowned for its expertise in healthcare, life sciences, and regulatory compliance, Wipro provides innovative solutions that help businesses transform. The Life Sciences division of Wipro plays a critical role in supporting global pharmaceutical and healthcare companies with their clinical research, regulatory submissions, and pharmacovigilance needs.
Job Responsibilities
As a Drug Safety Analyst – Literature Specialist at Wipro, you will:
1. Pharmacovigilance Data Management
- Oversee data acquisition and management for pharmacovigilance activities.
- Ensure compliance with regulatory and company standards.
2. Search Strategy Construction
- Build and execute efficient search strategies using biomedical databases and content aggregators like OVID, Embase, Medline, and PubMed.
3. Comprehensive Literature Review
- Perform detailed analyses of scientific literature to support regulatory submissions, safety assessments, and health agency requests.
4. Content Acquisition
- Stay updated with new technologies to enhance content acquisition processes.
5. Team Collaboration
- Collaborate with internal teams and external vendors to achieve business objectives and ensure process efficiency.
6. Innovation & Efficiency
- Drive innovative solutions to streamline pharmacovigilance processes, enhancing both literature searches and overall performance outcomes.
Key Qualifications
To be considered for this role, candidates must meet the following requirements:
| Qualification | Details |
|---|---|
| Educational Background | PhD, Pharm D, M.Pharm, B.Pharm, BDS, B.Tech/M.Tech (Life Sciences), M.Sc./B.Sc. in Life Sciences |
| Experience | Minimum of 4 years in pharmacovigilance |
| Specialized Experience | At least 1 year of hands-on experience with bibliographic databases such as OVID, Embase, Medline, and PubMed |
Required Skills
- Pharmacovigilance Expertise: Strong knowledge of the pharmaceutical industry, drug nomenclature, and product terminology.
- Bibliographic Database Proficiency: Experience in creating search strategies using OVID, Embase, Medline, PubMed, and other platforms.
- Scientific Literature Analysis: Ability to review and analyze scientific publications to meet regulatory requirements.
- Innovation and Efficiency: Passion for adopting new technologies and improving processes.
- Team Collaboration: Excellent interpersonal skills for working in cross-functional teams.
Why Join Wipro?
Working with Wipro offers you the chance to:
- Collaborate with industry-leading experts in pharmacovigilance and life sciences.
- Be part of innovative projects that contribute to global healthcare safety.
- Leverage cutting-edge technologies and methodologies to drive efficiencies in literature analysis.
How to Apply
If you meet the qualifications and are passionate about pharmacovigilance, apply today to join the Wipro team. Contribute to shaping the future of global healthcare and regulatory practices.
Meta Description:
Wipro hiring Drug Safety Analyst – Literature Specialist in Pune. 4+ yrs experience, life sciences background required. Apply now!