IQVIA Hiring for B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Lifesciences
| Position | Safety Associate |
|---|---|
| Location | Bangalore |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Lifesciences |
| Experience | 1-2 years in Pharmacovigilance |
| Salary Range | ₹4.5-6 Lakhs per annum |
| Database Expertise | Argus Database |
| Responsibilities | Case processing, adverse event reporting, compliance with global standards, team collaboration |
| Application | Email: subudhi.bhanuja@iqvia.com |
IQVIA Safety Associate Role: A Gateway to Pharmacovigilance Excellence
Are you ready to embark on a rewarding career with one of the world’s leading healthcare companies? IQVIA, renowned for its cutting-edge data analytics and life sciences services, is on the lookout for dedicated professionals to join its Pharmacovigilance (PV) team as a Safety Associate in Bangalore. Here’s why this role could be the stepping stone to your professional success.
Why Choose IQVIA?
IQVIA is more than just a company; it’s an innovator in the healthcare industry. With a focus on improving patient outcomes through data-driven insights and technological advancements, joining IQVIA means becoming a part of a transformative organization. As a Safety Associate, you will be working at the forefront of pharmacovigilance, ensuring drug safety and compliance with global standards.
Core Responsibilities
As a Safety Associate at IQVIA, your role will revolve around ensuring the safety of drugs through meticulous case processing. You will:
- Handle Adverse Event Reports: You will review and assess adverse drug event reports, contributing to patient safety.
- Database Management: Expertise in the Argus Database is critical, as you will process and manage safety data using this tool.
- Regulatory Compliance: Ensuring compliance with global pharmacovigilance regulations will be a key part of your day-to-day tasks.
- Collaboration: You’ll collaborate with cross-functional teams to support accurate data capture and reporting, both in clinical trials and post-marketing.
Qualifications That Set You Apart
To excel in this role, IQVIA is looking for professionals with:
- Pharmacovigilance Experience: A minimum of 1-2 years of experience in case processing within the pharmacovigilance domain.
- Argus Database Proficiency: Hands-on experience with the Argus Database is non-negotiable.
- Attention to Detail: In this role, precision is critical, as errors in safety reporting can have serious consequences.
- Strong Communication Skills: You’ll need excellent communication abilities to work closely with teams and stakeholders.
Why This Job Matters
In the ever-evolving healthcare landscape, the safety and efficacy of drugs are paramount. As a Safety Associate at IQVIA, you will be at the heart of this mission, ensuring that every drug released into the market meets the highest safety standards. Your work directly impacts patient health, making this more than just a job—it’s a responsibility to society.
Career Growth Opportunities
Working at IQVIA offers immense potential for career growth. The company is known for nurturing talent and providing opportunities for advancement within its global structure. Whether you aim to specialize further in pharmacovigilance or aspire to transition into other areas of clinical research, IQVIA offers a platform to grow.
Ready to Apply?
If you possess the qualifications and are eager to take on this pivotal role, don’t hesitate. Join a company that’s shaping the future of healthcare. Share your resume at subudhi.bhanuja@iqvia.com and take the first step towards a rewarding career with IQVIA.
For more details, visit the full job posting here.