Kickstart Your Pharmacovigilance Career: Veeda Lifesciences Hiring Associates (Hybrid Role)
Are you a recent B.Pharm or M.Pharm graduate eager to launch your career in the dynamic field of pharmacovigilance? Veeda Lifesciences is offering an exciting opportunity for aspiring Pharmacovigilance Associates to join their team in a hybrid work environment. This entry-level role provides a fantastic platform to gain hands-on experience and contribute to ensuring drug safety. If you’re passionate about pharmaceutical safety and possess strong analytical skills, this could be your ideal career move.
Why Choose Veeda Lifesciences?
Veeda Lifesciences is a leading Contract Research Organization (CRO) committed to delivering high-quality clinical research services. By joining their team, you’ll benefit from:
- Hybrid Work Model: Enjoy the flexibility of working both from home and the office.
- Career Growth: Gain valuable experience in a rapidly growing industry.
- Comprehensive Training: Develop your skills in pharmacovigilance principles and practices.
- Collaborative Environment: Work with experienced professionals in a supportive team.
(H2: Pharmacovigilance Associate: Job Responsibilities)
As a Pharmacovigilance Associate at Veeda Lifesciences, you will be involved in a variety of critical tasks, including:
(H3: Aggregate Reports)
- Collecting and preparing essential safety reports like Risk Management Plans (RMPs), Periodic Benefit-Risk Evaluation Reports (PBRERs/PSURs), Periodic Adverse Drug Experience Reports (PADERs), and addendums to clinical overview summaries.
- Collaborating with cross-functional teams to address and resolve issues during safety data review and report preparation.
- Ensuring timely submission of reports to maintain regulatory compliance.
(H3: Literature Search & Review)
- Establishing and implementing search strategies to monitor literature databases for relevant safety information.
- Performing initial reviews of literature articles, categorizing them into Individual Case Safety Reports (ICSRs), Adverse Events of Interest (AOIs), and other relevant classifications.
(H3: Triaging & Case Processing, Quality Check)
- Receiving, tracking, and triaging Individual Case Safety Reports (ICSRs).
- Conducting duplicate searches and ensuring case processing adheres to Standard Operating Procedures (SOPs).
- Reviewing case quality against source documents to maintain accuracy and compliance.
(H3: Medical Inquiry Management)
- Managing Medical Information Contact Center (MICC) activities.
- Responding to medical, pharmaceutical, and technical inquiries, including those related to adverse events (AEs).
- Maintaining detailed records and ensuring timely responses to all inquiries.
- Reporting adverse events to the case processing team.
(H2: Required Skills and Qualifications)
To excel in this role, you should possess:
- A Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm) degree, or a relevant qualification.
- A fundamental understanding of pharmacovigilance principles and regulatory guidelines.
- Familiarity with safety databases and literature search tools.
- Strong analytical and problem-solving skills.
- Excellent communication and documentation skills.
- 0-1 year of experience.
(H2: How to Apply)
If you’re ready to take the next step in your pharmacovigilance career, Veeda Lifesciences wants to hear from you!
Interested candidates can share their resumes at:
- Email: [email protected]
- Phone: 6359600877
(Conclusion)
This is an exceptional opportunity for recent graduates to enter the pharmacovigilance field with a reputable organization. Don’t miss your chance to join Veeda Lifesciences and contribute to the safety of pharmaceutical products. Apply today and embark on a rewarding career journey!
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