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Navatio Pharma, a fast-growing name in global pharmacovigilance, is hiring Drug Safety Associates – Literature Reviewers in Hyderabad. If you have a keen eye for detail, strong analytical skills, and experience in drug safety and literature surveillance, this is the perfect opportunity to take your PV career to the next level.
Job Overview
- Job Title: Drug Safety Associate – Literature Reviewer
- Location: Hyderabad, India
- Experience: 2–4 years
- Employment Type: Full-time
- Availability: Immediate joiners preferred
- Company: Navatio Pharma
- Application Deadline: 4 December 2025
Key Responsibilities
As a Drug Safety Associate – Literature Reviewer, you will play a crucial role in ensuring global patient safety by monitoring scientific literature for potential safety signals.
Your responsibilities include:
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- Conducting systematic literature searches for safety data and case reports.
- Reviewing and evaluating scientific articles for relevant adverse event information.
- Summarizing findings in compliance with pharmacovigilance regulations.
- Assisting in preparation of safety reports, aggregate reviews, and signal management documentation.
- Collaborating with cross-functional PV teams for data validation and quality assurance.
Required Qualifications
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field.
- 2–4 years of experience in pharmacovigilance or drug safety, with exposure to literature review.
- Excellent written and verbal communication skills.
- Strong analytical and research abilities.
- High attention to detail and ability to work independently.
Why Join Navatio Pharma?
- Be part of a dynamic global pharmacovigilance team.
- Opportunity to contribute to patient safety and regulatory compliance worldwide.
- Work in a collaborative, innovation-driven environment.
- Competitive salary and benefits package.
How to Apply
Interested candidates can send their updated resume to:
📧 hr@navatiopharma.com
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