Cencora PharmaLex Hiring Pharmacovigilance Jobs in Noida
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Educational Requirements
- Skills & Professional Competencies
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
Hiring Pharmacovigilance Specialist with life science degree. 1 vacancy in Noida for ICSR, risk management, safety reporting.
Cencora is hiring a Specialist in Pharmacovigilance Epidemiology & Risk Management for its consulting operations in Noida. This role is ideal for professionals seeking hands-on exposure to global drug safety, regulatory reporting, and real-world pharmacovigilance practices across clinical trials and post-marketing programs. You will work closely with cross-functional safety teams to ensure patient safety, regulatory compliance, and high-quality safety data management.
Company Overview
Cencora is a global healthcare services organization dedicated to creating healthier futures for people and animals worldwide. With a strong presence across pharmaceutical, biotechnology, and healthcare ecosystems, Cencora supports innovation, compliance, and patient safety throughout the product lifecycle.
Through its affiliated company, PharmaLex India Private Limited, Cencora delivers specialized consulting services in pharmacovigilance, regulatory affairs, epidemiology, and risk management. The organization is known for its ethical standards, global reach, and commitment to high-quality healthcare outcomes.
Job Role & Responsibilities
As a Specialist – Pharmacovigilance Epidemiology & Risk Management, you will play a critical role in safety case management, regulatory reporting, and quality assurance activities.
Key responsibilities include:
- Triage and initial validity assessment of safety cases from spontaneous reports, clinical trials, health authorities, and scientific literature
- Data entry and maintenance of Individual Case Safety Reports (ICSRs) in validated pharmacovigilance databases
- Initial ICSR assessment and evaluation of reportability requirements
- Assessment of expedited reporting obligations and applicable regulatory timelines
- Preparation of standard regulatory reporting forms such as CIOMS I, MedWatch, and XML files
- Generation and follow-up of safety queries to obtain complete and accurate case information
- Submission of ICSRs to health authorities and business partners
- Completion and documentation of safety cases in accordance with project requirements
- Quality checks and quality assurance of ICSRs to ensure compliance with industry standards and internal procedures
- Retrieval and review of cases from EVWEB and assessment of company versus non-company cases
- Mentoring and supporting new team members through process guidance and knowledge sharing
- Performing additional pharmacovigilance activities as assigned by the supervisor
Eligibility / Qualifications
Educational Requirements
- University degree in Life Sciences or a related scientific discipline
Relevant courses include: B.Sc Life Sciences, M.Sc Life Sciences, Pharmacy, Pharmacology, Biotechnology, Clinical Research, Public Health
Skills & Professional Competencies
- Basic experience in pharmacovigilance, drug safety, or a related healthcare field
- Strong attention to detail with a high focus on data quality and compliance
- Ability to manage multiple tasks, prioritize workload, and meet regulatory timelines
- Strong written and verbal communication skills with business-level English proficiency
- Confident professional presence with the ability to identify issues and propose solutions
- Willingness to learn and develop expertise through hands-on project exposure
Location & Salary
- Job Location: Noida, Uttar Pradesh (On-site)
- Employment Type: Full-time
- Salary: Competitive, aligned with industry standards and experience level
Application Process
Eligible candidates are encouraged to apply online through the official Cencora careers portal using the link below:
Shortlisted candidates will be contacted by the recruitment team for further steps in the hiring process.
Frequently Asked Questions (FAQs)
Is prior pharmacovigilance experience mandatory?
Basic experience or exposure to drug safety or related healthcare fields is preferred, but on-the-job learning is supported.
Does this role involve clinical trial safety cases?
Yes. The role includes safety cases from clinical trials, spontaneous reports, literature, and health authorities.
Is this a work-from-home position?
No. This role is based on-site in Noida.
Will I work on regulatory submissions?
Yes. The role involves preparation and submission of ICSRs and expedited safety reports.
Does Cencora support career growth in pharmacovigilance?
Yes. Cencora provides mentoring, structured learning, and exposure to global safety projects.
| Company | Cencora (PharmaLex India Private Limited) |
|---|---|
| Vacancies | 1 |
| Required Education | B.Sc/M.Sc Life Sciences, Pharmacy, Biotechnology |
| Experience | Entry-level to early career Pharmacovigilance experience |
To apply for this job please visit careers.cencora.com.
