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🚨 Hiring Alert: Pharmacovigilance Specialist 🚨
💼 Location: Bangalore, Kochi, Thane, Pune, Kolkata (Hybrid Mode)
📅 Experience Required: 3 – 5 years
🎓 Skills: Argus, Case Processing, Legal Case Processing, GVP
📧 Apply: Send your resume to bhavanasri.gundala@clinovo.com
Join Us as a Pharmacovigilance Specialist! 💊
Are you passionate about patient safety and eager to contribute to global healthcare solutions? We’re on the lookout for a Pharmacovigilance Specialist who’s skilled in Argus, case processing, and legal case processing. If you want to make a real difference in the field of pharmacovigilance, this role could be the perfect fit for you!
Why Should You Apply?
Imagine being at the forefront of patient safety, ensuring that every drug on the market is thoroughly vetted and safe for consumption. As a Pharmacovigilance Specialist, your role is critical to healthcare systems across the globe, and your work directly impacts lives. This is your chance to be part of something big!
What You’ll Do:
Your daily tasks will revolve around case processing and quality review, making sure every drug-related event is managed properly. From data entry to medical assessment, your work will ensure the safety of pharmaceutical products.
Let’s dive deeper into your key responsibilities!
Key Responsibilities 📝
- End-to-End Case Processing: You’ll handle the full cycle of case processing, including data entry, performing medical assessments, and conducting quality reviews. Every adverse event report will pass through your hands, ensuring that nothing slips through the cracks.
- Adverse Event Management Using Argus: You will work with the Argus system to manage and track adverse event reports. Your expertise will ensure that every report is thoroughly investigated and processed efficiently.
- Legal Case Processing: You’ll also work on legal case processing to make sure all cases comply with global pharmacovigilance regulations. Whether it’s FDA, EMA, or other regulatory bodies, your work ensures that we’re always on the right side of the law.
- Collaboration with Teams: You’ll partner with cross-functional teams, regulatory authorities, and external stakeholders to ensure that every drug is safe for consumers.
- Stay Updated on Global Regulations: In this fast-paced industry, staying on top of pharmacovigilance regulations and industry best practices is essential. You’ll be the go-to person for all things related to global regulatory frameworks like the FDA and EMA.
What We’re Looking For in You 🎯
This role is for someone with a sharp eye for detail, excellent problem-solving skills, and a passion for pharmacovigilance. Do you have experience in case processing and Argus? Do you understand legal case processing? If so, you’re already halfway there!
Here’s what we need:
- Proven Experience in Pharmacovigilance: You should have 3 to 5 years of experience in pharmacovigilance, with specific expertise in Argus and case processing.
- Knowledge of Legal Case Processing: Having experience with legal case processing is a must. You’ll need to ensure that every case aligns with global regulations and that all reports are compliant.
- Global Regulatory Knowledge: Familiarity with FDA, EMA, and other global regulatory frameworks is essential. The world of pharmacovigilance is constantly evolving, so you’ll need to stay updated on all the latest guidelines.
- Strong Communication Skills: You’ll be collaborating with different teams and external stakeholders, so excellent communication is key. You’ll need to present information clearly and effectively, both verbally and in writing.
- Attention to Detail: One small error can have huge consequences in this field. We’re looking for someone who can handle a fast-paced environment and pay attention to even the smallest details.
Why You’ll Love This Role 🌟
Working with us, you’ll be part of a dynamic and passionate team that prioritizes patient safety above all else. This is a hybrid role with locations across Bangalore, Kochi, Thane, Pune, and Kolkata, so you’ll have the flexibility to work in different cities while contributing to a global mission.
If you’re excited about the idea of using your pharmacovigilance expertise to make a positive impact on the world, we want to hear from you! Your work will not only ensure the safety of millions of patients, but you’ll also be part of a team that’s changing the face of global healthcare.
Ready to Apply? 📨
Don’t wait! If you have the skills and passion we’re looking for, send your resume to bhavanasri.gundala@clinovo.com and take the next step in your pharmacovigilance career.
