"Bristol Myers Squibb Hiring Senior Specialist – APMC Data Management in Hyderabad | Pharma Regulatory Jobs 2026"
Pharma Duniya is a trusted platform providing the latest pharma job updates, walk-in interviews, clinical research openings, and pharmacy career guidance. All job information is collected from official company websites and public sources. We do not charge any fees and are not official recruiters.
![]() |
(Cencora Hiring Senior Specialist – Case Processing in Noida) |
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.
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 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.
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.
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)
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.
University degree in Life Sciences, such as:
Pharmacy
Biotechnology
Clinical Research
Related scientific disciplines
Minimum 1.5 years of hands-on experience in:
ICSR case processing
Pharmacovigilance safety databases
Regulatory safety reporting
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
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 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.
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
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.
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.
No, this role requires at least 1.5 years of ICSR case processing experience.
Certification is not mandatory,y but relevant PV training is an added advantage.
Spontaneous, clinical trial, literature, and health authority ICSRs.
Yes, this is a full-time, permanent role.
Yes, the role involves global safety reporting and regulatory interactions.
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.
Kya aapka resume bar-bar reject ho raha hai?
Kya interview calls nahi aa rahi, chahe qualification aur skills ho?
Aaj ke competitive pharma job market me 90% resumes ATS (Applicant Tracking System) ke stage par hi reject ho jaate hain, kyunki:
Resume outdated format me hota hai
Pharma-specific keywords missing hote hain
HR-friendly & role-specific structure nahi hota
QA, QC, PV, Clinical Research roles ke hisaab se customisation nahi hoti
Pharma Duniya lekar aaya hai Professional Pharma Resume Writing Service, jo specially pharma & life science candidates ke liye design ki gayi hai.
✔ Fresher & Experienced candidates ke liye resume
✔ 100% ATS-friendly format
✔ HR-approved & industry-standard layout
✔ QA, QC, IPQA, Pharmacovigilance, Clinical Research, Regulatory Affairs ke hisaab se customisation
✔ Clear, clean & professional presentation
π Check Resume Writing Service:
π https://www.pharmaduniya.com/p/professional-pharma-resume-writing.html
π² WhatsApp support available for quick resume guidance
If you are preparing for pharma job interviews or actively searching for the latest QA, QC, Pharmacovigilance jobs and walk-in interviews, don’t miss these important and student-friendly career resources from Pharma Duniya π
Are you confused about which documents are required for pharma interviews? This complete checklist is specially designed for B.Pharm, M.Pharm, Pharm.D & Life Sciences candidates to avoid last-minute mistakes during interviews and walk-ins.
π See More:
https://www.pharmaduniya.com/2025/12/documents-required-for-pharma-interview.html
Pharma QA Interview Preparation for Freshers (Complete Guide) for B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences - Candidates who want to build a career in Quality Assurance (QA).
π Apply Here:
https://www.pharmaduniya.com/2026/01/pharma-qa-interview-preparation-for-freshers.html
Planning for industrial training or internship after B.Pharm, M.Pharm, or M.Sc? This complete student guide (2025-26) explains how to apply, where to apply, and how to get selected for pharma industrial training programs.
π See Full Guide:
https://www.pharmaduniya.com/2025/10/Industrial%20Training.html
If you want daily verified updates on QA, QC, Pharmacovigilance, Clinical Research, and Pharma Walk-In Interviews, join Pharma Duniya’s official channels and never miss an opportunity.
✅ Join our WhatsApp Group
✅ Join our Telegram Channel
π Get verified pharma job alerts, interview tips, resume guidance, and student career support directly on your phone.
π Visit daily: https://www.pharmaduniya.com