Pharmacovigilance Senior Research Scientist Hiring at Fresenius Kabi
- PV Jobs Gurgaon | Fresenius Kabi
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Educational Requirements
- Experience Requirements
- Skill Requirements
- Location & Salary
- Application Process
- FAQs
- Who can apply for this pharmacovigilance role?
- Is experience in ICSR processing mandatory?
- Is this a remote position?
- What is the maximum notice period accepted?
- How do I apply?
PV Jobs Gurgaon | Fresenius Kabi
Fresenius Kabi hiring Senior Research Scientist – Pharmacovigilance in Gurgaon. M.Pharm/PharmD
Fresenius Kabi Oncology is hiring an experienced Senior Research Scientist – Pharmacovigilance (PV Operations) for its Gurgaon location. This role is suited for qualified pharmacovigilance professionals with hands-on experience in ICSR processing, case triage, data entry, and quality control. Candidates with a strong background in drug safety operations and global PV compliance will find this opportunity aligned with long-term career growth in regulated pharmaceutical environments.
Company Overview
Fresenius Kabi is a global healthcare company specializing in lifesaving medicines, infusion therapies, clinical nutrition, and oncology products. With a strong presence across regulated markets, Fresenius Kabi is recognized for its commitment to patient safety, regulatory compliance, and high-quality pharmaceutical manufacturing.
The company’s oncology and drug safety operations play a critical role in ensuring continuous monitoring of product safety across global markets. Careers at Fresenius Kabi offer professionals exposure to international pharmacovigilance standards, robust quality systems, and collaboration with cross-functional global teams.
Job Role & Responsibilities
The Senior Research Scientist – Pharmacovigilance will be responsible for end-to-end PV operational activities, ensuring accurate and compliant handling of adverse event data.
Key responsibilities include:
- Processing Individual Case Safety Reports (ICSRs) in compliance with global pharmacovigilance regulations
- Performing case triage, data entry, and quality control activities across safety databases
- Reviewing and validating adverse event reports from clinical trials, post-marketing sources, and literature
- Ensuring compliance with global drug safety regulations and internal SOPs
- Supporting signal detection inputs and safety data trend analysis
- Collaborating with global PV, regulatory affairs, and medical teams
- Supporting audits, inspections, and responses to regulatory authority queries
- Maintaining high standards of data accuracy, completeness, and timeliness
- Contributing to process improvement initiatives within PV Operations
This role directly supports patient safety, regulatory compliance, and the benefit–risk assessment of oncology products.
Eligibility / Qualifications
Educational Requirements
- M.Pharm or Pharm.D (mandatory)
Relevant courses include: M.Pharm Pharmacology, M.Pharm Pharmacy Practice, Pharm.D, Clinical Pharmacy, Drug Safety and Pharmacovigilance
Experience Requirements
- 3 to 6 years of experience in pharmacovigilance or drug safety operations
- Hands-on experience in ICSR processing, case triage, data entry, and QC
Skill Requirements
- Strong knowledge of global pharmacovigilance regulations and guidelines
- Experience working with safety databases and PV workflows
- Excellent attention to detail and documentation accuracy
- Strong analytical and communication skills
- Ability to work in cross-functional and global team environments
Location & Salary
- Job Location: Gurgaon, India
- Work Mode: Office-based (with one day flexible working)
- Job Type: Full-Time
Application Process
Eligible candidates are requested to share their updated resumes via email.
Apply via Email: Leela.Pant@fresenius-kabi.com
Candidates should mention “Senior Research Scientist – Pharmacovigilance” in the subject line for faster screening.
FAQs
Who can apply for this pharmacovigilance role?
Candidates with M.Pharm or Pharm.D qualifications and 3–6 years of PV experience can apply.
Is experience in ICSR processing mandatory?
Yes. Hands-on experience in ICSR processing and PV operations is required.
Is this a remote position?
No. This is an office-based role with one day of flexible working.
What is the maximum notice period accepted?
Candidates with a notice period of up to 2 months are eligible.
How do I apply?
Send your resume to Leela.Pant@fresenius-kabi.com.
| Company | Fresenius Kabi |
|---|---|
| Vacancies | Senior Research Scientist – Pharmacovigilance |
| Required Education | M.Pharm / Pharm.D |
| Experience | 3–6 years |
To apply for this job email your details to Leela.Pant@fresenius-kabi.com
