Wipro Hiring for Drug Safety Analyst – Literature Specialist
Key Points
| 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 |
| Salary | INR 5,80,000 – INR 10,00,000 |
| Location | Pune |
Exciting Opportunity as a Drug Safety Analyst at Wipro
Are you ready to take your career in pharmacovigilance to the next level? Wipro, a global leader in technology and consulting services, is seeking passionate individuals to join their team as Drug Safety Analysts – Literature Specialists in Pune. This position provides a unique opportunity to engage with the healthcare and pharmaceutical industry, applying your expertise in scientific literature analysis and pharmacovigilance processes to make a difference.Wipro Hiring for Drug Safety Analyst – Literature Specialist
Why Wipro?
Wipro Limited stands as one of the foremost global IT, consulting, and business process services companies. With a workforce of over 200,000 professionals and a presence in more than 50 countries, Wipro delivers a diverse array of services in IT, healthcare, and life sciences. Their commitment to innovation and excellence allows them to provide transformative solutions that address the complexities of today’s business environment. In particular, Wipro’s Life Sciences division plays a crucial role in supporting global pharmaceutical companies through clinical research, regulatory compliance, and pharmacovigilance.
Key Responsibilities of the Role
As a Drug Safety Analyst – Literature Specialist, you will be entrusted with critical responsibilities that are essential for maintaining the safety and efficacy of pharmaceutical products:
- Pharmacovigilance Data Management: You will oversee the execution of data acquisition and management processes for pharmacovigilance activities, ensuring that all data is handled with the utmost accuracy and compliance.
- Search Strategy Construction: Your expertise will come into play as you build and execute efficient search strategies on various biomedical databases and content aggregator platforms, crucial for thorough literature reviews.
- Comprehensive Literature Review: Perform in-depth analysis and reviews of scientific publications to support regulatory submissions and requests from health agencies. Your analytical skills will directly contribute to improving patient safety.
- Content Acquisition: Staying updated on the latest technologies and methodologies will allow you to enhance content acquisition processes, ensuring the most relevant and impactful information is utilized.
- Team Collaboration: Liaising with internal and external teams, including vendors, will be an essential part of your role. This collaboration is key to meeting business objectives and ensuring process efficiency.
- Innovation & Efficiency: Your innovative mindset will drive the development of solutions that streamline processes, improve outcomes in literature searches, and enhance pharmacovigilance activities.
Qualifications: Are You the Right Fit?
To thrive in this position, you should have the following qualifications:
- Educational Background: A PhD, Pharm D, M.Pharm, B.Pharm, BDS, B.Tech/M.Tech in Life Sciences, or an M.Sc./B.Sc. in Life Sciences.
- Experience: A minimum of 4 years in pharmacovigilance, with at least 1 year of hands-on experience in bibliographic databases and search libraries such as OVID, Embase, Medline, and PubMed.
Essential Skills for Success
The ideal candidate for this role should possess a blend of skills that will enable them to excel:
- Pharmacovigilance Expertise: A strong foundation in the pharmaceutical industry, drug nomenclature, and product terminology is vital.
- Bibliographic Database Proficiency: Experience in constructing and executing search strategies on leading search platforms will set you apart.
- Scientific Literature Analysis: Proven ability to review and analyze scientific publications to meet regulatory needs is crucial for this role.
- Innovative Mindset: An eagerness to embrace the latest technologies and methodologies will help you drive efficiencies and improve processes.
- Team Collaboration: Strong interpersonal skills will be essential for effective collaboration with cross-functional teams and external vendors.
Your Career Journey Awaits
Joining Wipro as a Drug Safety Analyst – Literature Specialist offers a fantastic opportunity to expand your knowledge and skills in pharmacovigilance. You’ll be part of a dedicated team that is committed to enhancing patient safety and ensuring the efficacy of pharmaceutical products. This role not only promises professional growth but also allows you to contribute meaningfully to the healthcare sector.
How to Apply
If this role excites you and you believe you have what it takes, don’t miss out on this opportunity. Apply through Wipro’s official career portal to take the first step toward a rewarding career in pharmacovigilance. This is your chance to make a lasting impact in the healthcare industry while developing your skills in a dynamic and supportive environment.
Application link
Join Wipro today and embark on a journey that will shape your future in pharmacovigilance!