Fresher Pharmacovigilance Associate Required at Vantive Gurgaon
- Pharmacovigilance Associate Required at Vantive Gurgaon
- About Vantive
- Job Details
- Position: Pharmacovigilance Associate
- Key Responsibilities
- Qualifications & Requirements
- Education:
- Experience:
- Key Skills:
- How to Apply?
- Company & Job Overview Table
Pharmacovigilance Associate Required at Vantive Gurgaon
Vantive, a global leader in kidney care and vital organ therapies, is looking for a Pharmacovigilance Associate to join its Patient Safety team in Gurgaon, Haryana. If you are passionate about drug safety and regulatory compliance, this opportunity is for you! Read on to learn about the job role, required qualifications, and how to apply.
About Vantive
For over 70 years, Vantive has been at the forefront of kidney care innovations. The company is now expanding into vital organ therapies, aiming to enhance patient lives through digital solutions and advanced healthcare services.
📄 Get Your Dream Job with a Professional Resume!
💼 Struggling to Get Noticed by Recruiters? 📄 Let Professionally Crafted Resumes Boost Your Career! 🚀
📱 Get More DetailsJoin Vantive to be part of a team that values innovation, patient safety, and quality healthcare.
Job Details
Position: Pharmacovigilance Associate
Location: Gurgaon, Haryana, India
Job Category: Patient Safety
Job Code: JR – 157604
Date Posted: 13th March 2025
Key Responsibilities
Pharmacovigilance Quality Systems
- Ensure compliance with Baxter Pharmacovigilance Quality Systems and policies.
- Maintain proper document management, retention, and archiving.
- Complete all necessary training and certification requirements.
- Adhere to the Business Continuity Plan (BCP) and compliance guidelines.
Case Intake & Safety Monitoring
- Handle adverse event (AE) and pregnancy report collection in the Pharmacovigilance safety database.
- Process reports from patients, healthcare professionals, social media, and partner companies.
- Perform initial assessment, duplicate checks, case validity checks, and seriousness assessments.
- Capture all source documents and ensure proper data entry.
- Coordinate with global teams for follow-up information and case completion.
Safety Risk Management & Compliance
- Assist in implementing risk minimization measures.
- Conduct safety surveillance activities for new potential risks.
- Escalate regulatory requests and safety concerns to the Qualified Officer In Charge.
Qualifications & Requirements
Education:
Candidates must have a degree in one of the following fields:
- B.Pharm / M.Pharm (Pharmacy)
- B.Sc / M.Sc (Life Sciences, Biotechnology, Microbiology, Biochemistry)
- MBBS / BDS / BHMS / BAMS (Medical & Healthcare Fields)
Experience:
- 0-3 years of experience in Pharmacovigilance, Drug Safety, or Clinical Research.
- Experience in Pharmacovigilance databases and case processing is a plus.
Key Skills:
- Strong understanding of Pharmacovigilance regulations and safety monitoring.
- Excellent communication and analytical skills.
- Ability to work in cross-functional teams.
- Knowledge of global regulatory guidelines (ICH-GCP, US FDA, EMA, MHRA).
How to Apply?
Interested candidates can apply online by clicking the link below:
👉 Apply Now
📅 Deadline: Apply ASAP as vacancies are filling fast!
Company & Job Overview Table
| Company Name | Current Vacancies | Required Education | Experience Required |
|---|---|---|---|
| Vantive | Pharmacovigilance Associate | B.Pharm, M.Pharm, B.Sc, M.Sc, MBBS, BDS, BHMS, BAMS | 0-3 years |
Boost your career with Vantive and make a real impact in Pharmacovigilance & Patient Safety! Apply now and be a part of the future of vital organ therapies. 🚀
To apply for this job please visit jobs.vantive.com.