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"Cencora Hiring Senior Specialist – Case Processing in Noida | Pharmacovigilance Jobs"

"Cencora Hiring Senior Specialist – Case Processing in Noida | Pharmacovigilance Jobs."




(Cencora Hiring Senior Specialist – Case Processing in Noida)




Introduction

Pharmacovigilance has become one of the most critical functions in the pharmaceutical and healthcare industry, ensuring patient safety and regulatory compliance across global markets. With increasing regulatory scrutiny and rising safety data volumes, skilled professionals in ICSR case processing and safety reporting are in high demand.

In this context, Cencora, through its affiliate PharmaLex India Private Limited, has announced an exciting career opportunity for the role of Senior Specialist – Case Processing at its Noida location. This full-time role is ideal for life science professionals looking to advance their careers in pharmacovigilance, drug safety, and global regulatory operations.


About the Company – Cencora

Cencora is a globally recognized healthcare solutions organization focused on improving patient outcomes by ensuring safe, effective, and compliant use of medicines. The company provides integrated services across pharmaceutical commercialization, regulatory affairs, pharmacovigilance, and healthcare data management.

Company Overview

  • Company Name: Cencora

  • Headquarters: United States

  • Founded: 2023 (rebranded from AmerisourceBergen)

  • Employees: 40,000+ worldwide

  • Industry: Healthcare Services, Pharmaceutical Solutions

  • Indian Operations: Through affiliates like PharmaLex India Private Limited

Cencora supports global pharmaceutical companies throughout the product lifecycle, with a strong emphasis on drug safety, regulatory compliance, and patient-centric solutions.


Job Overview Summary

The Senior Specialist – Case Processing role at Cencora is a core pharmacovigilance position responsible for managing Individual Case Safety Reports (ICSRs) from multiple sources. The role involves end-to-end safety case processing, regulatory submissions, quality control, and mentoring junior team members.

This position offers exposure to global safety databases, international regulatory requirements, and high-quality PV operations, making it a strong career move for experienced case processing professionals.


Vacancy Details (Official)

  • Job Title: Senior Specialist – Case Processing

  • Company: Cencora (PharmaLex India Private Limited)

  • Employment Type: Full-time, Permanent

  • Job Location: Noida, Uttar Pradesh, India

  • Department: Pharmacovigilance / Drug Safety

  • Experience Required: Minimum 1.5 years

  • Mode of Work: On-site / Hybrid (as per company policy)


Job Role & Responsibility Explanation

As a Senior Specialist in Case Processing, you will play a vital role in ensuring accurate, timely, and compliant safety reporting. Your responsibilities include:

  • Reviewing and triaging safety information from multiple sources

  • Performing initial case validity assessment for spontaneous, clinical trial, literature, and health authority cases

  • Processing ICSRs in pharmacovigilance safety databases with high data quality

  • Assessing cases for expedited and non-expedited reporting requirements

  • Preparing CIOMS I forms, MedWatch reports, and XML submissions

  • Managing follow-up requests and ensuring timely case closure

  • Submitting safety reports to global health authorities and partners

  • Conducting quality checks (QC) to ensure regulatory compliance

  • Performing EVWEB searches and company vs non-company case assessments

  • Supporting workload allocation and mentoring junior associates

  • Participating in continuous improvement initiatives within PV operations

This role demands accuracy, regulatory knowledge, and strong ownership of safety data.


Eligibility Criteria (Official)

Educational Qualification

  • University degree in Life Sciences, such as:

    • Pharmacy

    • Biotechnology

    • Clinical Research

    • Related scientific disciplines

Experience Requirement

  • Minimum 1.5 years of hands-on experience in:

    • ICSR case processing

    • Pharmacovigilance safety databases

    • Regulatory safety reporting


Skills Required

To succeed in this role, candidates should possess:

  • Strong understanding of pharmacovigilance workflows

  • Knowledge of global regulatory timelines and reporting standards

  • close attention to detail and quality orientation

  • Ability to manage multiple cases independently

  • Strong written and verbal English communication skills

  • Experience with safety databases and PV tools

  • Team collaboration and mentoring capabilities

  • Time management and prioritization skills


Salary Estimate (Indicative)

  • Estimated Salary Range: ₹6,00,000 – ₹9,00,000 per annum

  • Salary may vary based on:

    • Experience level

    • PV database expertise

    • Interview performance

    • Internal company policies

Additional benefits and learning opportunities are provided as per role eligibility.


Interview Details (Official)

  • Interview Mode: Online / Virtual (initial rounds)

  • Selection Process:

    • Resume shortlisting

    • Technical interview (Pharmacovigilance & ICSR knowledge)

    • HR discussion

Shortlisted candidates will be contacted directly by the recruitment team.


Required Documents 

Candidates should keep the following documents ready:

  • Updated resume / CV

  • Educational qualification certificates

  • Experience certificates (if applicable)

  • Government-issued ID proof

  • Any relevant pharmacovigilance training certificates


Job Location

  • City: Noida

  • State: Uttar Pradesh

  • Country: India

Noida is a major hub for pharmacovigilance, clinical research, and global pharma services, offering excellent career growth opportunities.


How to Apply 

Interested and eligible candidates can apply online through the official link:

Application Link:
https://myhrabc.wd5.myworkdayjobs.com/en-US/Global/job/Senior-Specialist-Case-Processing_R26664

Apply early to increase your chances of shortlisting.


FAQs – Cencora Senior Specialist Case Processing Job

Q1. Is this role suitable for freshers?

No, this role requires at least 1.5 years of ICSR case processing experience.

Q2. Is pharmacovigilance certification mandatory?

Certification is not mandatory,y but relevant PV training is an added advantage.

Q3. What type of cases will be handled?

Spontaneous, clinical trial, literature, and health authority ICSRs.

Q4. Is this a permanent position?

Yes, this is a full-time, permanent role.

Q5. Does Cencora provide global exposure?

Yes, the role involves global safety reporting and regulatory interactions.


Final Conclusion

The Senior Specialist – Case Processing role at Cencora offers an excellent opportunity for pharmacovigilance professionals to work in a globally respected healthcare organization. With exposure to international safetyreporting, a strong compliance culture, and career development opportunities, this position is ideal for candidates looking to grow in drug safety and regulatory operations.

If you have experience in ICSR processing and a passion for patient safety, this opportunity can be a strong step forward in your pharmacovigilance career.

Note: Pharma Duniya does not charge any money for job information.
Candidates are advised to verify details from the official company website.


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