Pharmacovigilance Vacancies in Noida: Clinical Safety/Clinical Trial ICSR Data Entry
Pharmacovigilance Vacancies in Noida: Clinical Safety/Clinical Trial ICSR Data Entry including SAEs/SUSARs
About Cencora PharmaLex India
Cencora PharmaLex India is a prominent name in the pharmaceutical industry, dedicated to ensuring drug safety and regulatory compliance. With a focus on excellence and innovation, we offer a dynamic work environment that fosters growth and development.
Cencora PharmaLex India Vacancies List
- Position Title: Pharmacovigilance Associate
- Company Name: Cencora PharmaLex India
- Salary: Competitive
- Company Address: Noida, Uttar Pradesh
- Industry Type: Pharmaceutical
- Department: Pharmacovigilance
- Employment Type: Full Time
- Role Category: Clinical Safety
- Educational Background Required: Bachelor’s/Master’s degree in Pharmacy/Life Sciences
- Key Skills: Clinical Safety, Case Processing, SAEs/SUSARs, EDC/Clinical Databases
📄 Get Your Dream Job with a Professional Resume!
💼 Struggling to Get Noticed by Recruiters? 📄 Let Professionally Crafted Resumes Boost Your Career! 🚀
📱 Get More DetailsJob Description
As a Pharmacovigilance Associate at Cencora PharmaLex India, you will be responsible for clinical safety and clinical trial ICSR data entry, including SAEs/SUSARs. Key responsibilities include:
About the Department & Responsibilities
The Pharmacovigilance department plays a crucial role in ensuring the safety of pharmaceutical products throughout their lifecycle. As a Pharmacovigilance Associate, you will be involved in end-to-end case processing, narrative writing, and submission of safety reports to regulatory authorities. You will collaborate with cross-functional teams to ensure compliance with regulatory requirements and facilitate timely reporting of adverse events.
Qualifications and Requirements
To qualify for the Pharmacovigilance Associate position, candidates must possess:
- Educational Background: Bachelor’s/Master’s degree in Pharmacy/Life Sciences
- Minimum Mandatory Experience: 1-3 years in clinical safety or pharmacovigilance
- Proficiency in clinical trial ICSR data entry, including SAEs/SUSARs
- Experience in narrative writing and case processing
- Strong communication and organizational skills
- Ability to work effectively in a fast-paced environment and prioritize tasks
How to Apply
If you meet the qualifications and are ready to take on this exciting opportunity, please email your application to aashi.jain@pharmalex.com. Be sure to include your resume and a cover letter highlighting your relevant experience and why you are interested in joining our team.