Pharmacovigilance Literature Surveillance Reconciliation Analyst Job at Merck in Bangalore for experienced PV professionals with global drug safety exposure.
Job Title: Literature Surveillance and Reconciliation Analyst
Company: Merck Ltd
Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Work Model: Office-based / Hybrid (as per business needs)
Industry: Pharmacovigilance / Patient Safety / Drug Safety
Experience Required: 3+ Years
Job Status: Active
Merck is hiring an experienced Literature Surveillance and Reconciliation Analyst for its Global Patient Safety operations in Bangalore. This role is designed for pharmacovigilance professionals with strong expertise in literature safety surveillance, ICSR reconciliation, and global regulatory compliance. The position offers exposure to international safety systems and collaboration with global stakeholders in a highly regulated research-driven environment. Pharmacovigilance Literature Surveillance Reconciliation Analyst Job
About the Company
Merck is a global science and technology leader operating across Healthcare, Life Science, and Electronics sectors. With a long-standing legacy of innovation and responsibility, Merck focuses on improving lives through scientific excellence. Its Global Patient Safety organization plays a critical role in monitoring the safety of medicinal products throughout development and post-marketing stages, ensuring compliance with international regulatory standards.
Working at Merck provides professionals with exposure to global pharmacovigilance frameworks, robust quality systems, and a culture that promotes integrity, inclusion, and continuous learning. Pharmacovigilance Literature Surveillance Reconciliation Analyst Job
Job Details
- Job Title: Literature Surveillance and Reconciliation Analyst
- Company Name: Merck Ltd
- Job Location: Bangalore, Karnataka
- Employment Type: Full-Time
- Functional Area: Pharmacovigilance / Global Patient Safety
- Experience Level: Minimum 3 years
- Education Requirement: Medical or Scientific Degree
Job Description
The Literature Surveillance and Reconciliation Analyst will support global literature surveillance operations and safety reconciliation activities within Merck’s Global Patient Safety ICSR Management team. The role focuses on maintaining data quality, regulatory compliance, and inspection readiness by ensuring accurate tracking and reconciliation of literature-derived safety information. Pharmacovigilance Literature Surveillance Reconciliation Analyst Job
Key Responsibilities
Literature Surveillance Operations
- Support literature surveillance processes as per global SOPs
- Perform reconciliation and quality control of non-ICSR literature data
- Upload, track, and manage scientific articles in safety databases
- Conduct quality checks to ensure data accuracy, completeness, and compliance
ICSR Reconciliation & Safety Monitoring
- Perform ICSR reconciliation across relevant safety systems
- Conduct quality monitoring and spot checks of safety data
- Ensure alignment between literature cases and ICSR records
- Support inspection readiness and ongoing PV compliance
Systems, Training & Access Management
- Maintain training documentation related to literature surveillance
- Support user access management for safety databases
- Ensure system documentation aligns with SOPs and regulatory expectations
Communication & Coordination
- Monitor team mailboxes and respond to safety-related requests
- Coordinate with global stakeholders and cross-functional teams
- Support smooth communication across matrix and international teams
Pharmacovigilance Literature Surveillance Reconciliation Analyst Job
Skills / Qualifications
Educational Qualification
Candidates must hold a medical or scientific degree, such as:
MBBS, B.Pharm, M.Pharm, PharmD, MSc Life Sciences, MSc Pharmacology, MSc Clinical Research, or PhD Life Sciences.
Pharmacovigilance Literature Surveillance Reconciliation Analyst Job
Experience Requirements
- Minimum 3 years of experience in Pharmacovigilance or Patient Safety
- Prior experience in literature surveillance and ICSR reconciliation
- Hands-on exposure to global drug safety regulations
- Experience with safety databases; ArisG exposure is an advantage
Pharmacovigilance Literature Surveillance Reconciliation Analyst Job
Key Skills
- Strong understanding of global PV regulations and guidelines
- Knowledge of safety requirements for clinical and post-marketing products
- Excellent written and verbal communication skills
- Strong attention to detail and quality-focused mindset
- Ability to work in global, cross-cultural environments
Pharmacovigilance Literature Surveillance Reconciliation Analyst Job
Benefits / Perks
- Competitive salary aligned with industry standards
- Exposure to global pharmacovigilance systems and operations
- Opportunity to work with international patient safety teams
- Strong learning environment with long-term career growth
- Inclusive and professional work culture
Pharmacovigilance Literature Surveillance Reconciliation Analyst Job
Why You Should Join
Joining Merck means becoming part of a globally respected organization committed to patient safety and scientific excellence. This role offers a strong platform to advance your career in pharmacovigilance, literature surveillance, and global safety leadership, with opportunities to grow into senior patient safety and regulatory roles. Pharmacovigilance Literature Surveillance Reconciliation Analyst Job
How to Apply
Interested candidates should apply through the official Merck career portal using the link below:
FAQs
Who can apply for this role?
Candidates with a medical or scientific degree and at least 3 years of pharmacovigilance experience.
Is this role suitable for freshers?
No, prior experience in literature surveillance or ICSR reconciliation is required.
Does this role involve ICSR processing?
The role focuses on reconciliation and quality monitoring rather than full end-to-end case processing.
Is international exposure involved?
Yes, the role involves collaboration with global patient safety teams.
What are the career growth opportunities?
This role can lead to senior positions in global patient safety, signal management, and pharmacovigilance leadership.
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