Cencora, a global leader in healthcare solutions, is seeking a Senior Specialist, Pharmacovigilance (PMO) to join their Noida office. This role is ideal for professionals passionate about pharmacovigilance program management, project coordination, and process optimization in clinical research. If you are organized, analytical, and thrive in fast-paced environments, this opportunity is perfect for you.
Key Responsibilities
As a Senior Specialist (PMO), you will:
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- Support program management for large-scale outsourcing projects.
- Monitor and prepare project controlling, reporting, and overall budget tracking.
- Identify and report potential budget discrepancies to the Program Manager.
- Track and report key performance indicators (KPIs).
- Manage timesheet activities in PLx Time Tracking & Accounting System.
- Maintain program-related projects operationally in PLx.
- Support onboarding/offboarding of internal and external resources.
- Compile regular customer checkpoint presentations.
- Ensure transparent reporting and timely monthly/quarterly financial statements.
- Assist in providing proper training, guidance, and working conditions for project staff.
- Continuously improve and harmonize internal pharmacovigilance processes.
Critical Qualifications & Skills
- Bachelor’s or Master’s degree in Sciences or Economics.
- High service orientation and client-focused mindset.
- Strong affinity for complex business and clinical processes.
- Ability to analyze, adapt, streamline, and increase process efficiency.
- Experience in supervising multiple projects simultaneously.
- Excellent team player with problem-solving skills.
- Structured, analytical, and independent work style.
- Proficient in MS Office, ERP, project management tools, and databases (Excel expertise preferred).
- Very good command of English, both written and spoken.
Benefits
- Competitive salary range: INR 8,00,000 – 12,00,000 per annum (depending on experience).
- Full-time permanent role in a global healthcare leader.
- Dynamic, collaborative, and inclusive work environment.
- Opportunity to work on large-scale pharmacovigilance programs.
- Career growth in clinical research and pharmacovigilance program management.
How to Apply
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