Cencora Hiring Senior Specialist Pharmacovigilance
- Cencora Hiring Senior Specialist Pharmacovigilance – 2+ Years Experience | Noida Location | Apply Now
- Company Overview
- Job Role & Responsibilities
- Core Pharmacovigilance Responsibilities
- ICSR & Regulatory Activities
- Project & Stakeholder Management
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Skills Required
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- 1. What is the required experience for this role?
- 2. What qualifications are required?
- 3. What are the main responsibilities?
- 4. Is this a good career opportunity?
- 5. What skills are essential for selection?
- Summary Table
Cencora Hiring Senior Specialist Pharmacovigilance – 2+ Years Experience | Noida Location | Apply Now
Cencora is hiring Senior Specialist Pharmacovigilance professionals for its consulting division in Noida, India. This is a full-time opportunity for candidates with at least 2 years of experience in pharmacovigilance, drug safety, and clinical research operations. The role focuses on literature screening, ICSR processing, and regulatory compliance, making it ideal for professionals looking to advance in high-paying pharma safety and regulatory careers.
Company Overview
Cencora is a globally recognized healthcare solutions provider committed to improving patient outcomes and advancing pharmaceutical innovation. With a strong presence across clinical research, drug safety, regulatory consulting, and healthcare services, Cencora plays a critical role in supporting pharmaceutical and biotechnology companies worldwide.
The organization is known for its robust compliance framework, global pharmacovigilance expertise, and commitment to ethical healthcare practices. Through its affiliated entity PharmaLex India Private Limited, Cencora delivers specialized regulatory and safety services that directly impact patient safety and drug lifecycle management.
Job Role & Responsibilities
As a Senior Specialist in Pharmacovigilance, you will handle critical drug safety operations, including medical literature monitoring, adverse event reporting, and regulatory documentation. This role demands precision, regulatory awareness, and strong analytical capabilities.
Core Pharmacovigilance Responsibilities
- Perform scientific literature screening using internal tools and external databases
- Identify and classify safety-relevant publications related to adverse drug reactions
- Manage literature tracking and documentation processes
- Enter validated safety data into pharmacovigilance safety databases
- Prepare regulatory reporting forms such as CIOMS I, MedWatch, and XML submissions
- Complete case processing and ensure accurate safety documentation
ICSR & Regulatory Activities
- Download and review Individual Case Safety Reports (ICSRs) from EMA Medical Literature Monitoring (MLM) services
- Conduct duplicate checks and ensure data consistency across safety systems
- Maintain compliance with global pharmacovigilance regulations and reporting standards
- Support regulatory submissions and documentation aligned with international guidelines
Project & Stakeholder Management
- Act as a key point of contact for clients and project stakeholders
- Collaborate with cross-functional teams in clinical research and drug safety
- Support additional pharmacovigilance and regulatory activities as required
Eligibility / Qualifications
Educational Qualification
Candidates must hold a degree in Life Sciences or related healthcare disciplines.
Required courses include:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Clinical Research, Nursing
Experience
- Minimum 2 years of experience in pharmacovigilance or drug safety
- Strong understanding of ICSR processing, literature review, and regulatory reporting
Skills Required
- Strong communication and presentation skills
- Knowledge of global pharmacovigilance regulations and safety databases
- Ability to manage multiple tasks and meet regulatory timelines
- Analytical thinking and attention to detail
Location & Salary
- Job Location: Noida, India
- Employment Type: Full-time
- Salary: Competitive salary package based on experience and industry standards in pharmacovigilance and clinical research
Application Process
Interested candidates can apply directly through the official Cencora careers portal:
Apply Here: https://careers.cencora.com/us/en/job/CHKCENUSR264423EXTERNALENUS/Senior-Specialist-Pharmacovigilance
Frequently Asked Questions (FAQs)
1. What is the required experience for this role?
Candidates must have at least 2 years of experience in pharmacovigilance or drug safety.
2. What qualifications are required?
A degree in Life Sciences, Pharmacy, Biotechnology, or related fields is required.
3. What are the main responsibilities?
The role involves literature screening, ICSR processing, regulatory reporting, and safety data management.
4. Is this a good career opportunity?
Yes. It offers strong career growth in pharmacovigilance, regulatory affairs, and clinical research with a global healthcare leader.
5. What skills are essential for selection?
Candidates need strong communication skills, regulatory knowledge, and attention to detail in safety data handling.
Summary Table
| Category | Details |
|---|---|
| Company | Cencora |
| Vacancies | Senior Specialist Pharmacovigilance |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Clinical Research, Nursing |
| Experience | 2+ Years Pharmacovigilance Experience |
To apply for this job please visit careers.cencora.com.
