Merck hiring Pharmacovigilance Literature Surveillance & Reconciliation Analyst

Literature Surveillance Analyst Vacancy Bangalore | PV

Merck hiring Literature Surveillance & Reconciliation Analyst in Bangalore. Pharmacovigilance professionals with 3+ years experience.

Merck is hiring a Literature Surveillance and Reconciliation Analyst for its R&D Excellence Center in Bangalore. This full-time role is ideal for experienced pharmacovigilance professionals who have worked in literature safety surveillance, ICSR reconciliation, and global patient safety operations. The position offers direct exposure to global drug safety systems, regulatory compliance, and cross-functional collaboration in an international research-driven environment.

This opportunity is well suited for candidates looking to strengthen their long-term career in pharmacovigilance, patient safety, and regulatory compliance within a globally respected life science organization.

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Company Overview

Merck is a global science and technology company operating across Healthcare, Life Science, and Electronics. With a strong heritage of innovation and responsibility, Merck focuses on advancing human progress through science-driven solutions that improve lives worldwide.

The company’s Global Patient Safety teams play a critical role in ensuring the safe development and post-authorization monitoring of medicinal products. Merck operates under stringent global regulatory frameworks and maintains high standards of quality, compliance, and scientific integrity across its R&D and post-marketing activities.

Working at Merck offers professionals exposure to international safety operations, robust regulatory systems, and a culture that values diversity, inclusion, and continuous learning.

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Job Role & Responsibilities

The Literature Surveillance and Reconciliation Analyst will be part of the Global Patient Safety ICSR Management team and will support literature surveillance processes, reconciliation activities, and safety data quality management.

Literature Surveillance Operations

• Support the business process owner for literature surveillance activities
• Perform operational tasks in the literature surveillance database, including reconciliation and quality control of non-ICSR literature
• Upload, manage, and track scientific articles in safety databases
• Conduct quality checks to ensure completeness, accuracy, and regulatory compliance of literature safety data

ICSR Reconciliation and Safety Monitoring

• Perform ICSR reconciliation activities across relevant safety systems
• Conduct quality monitoring and spot checks of safety information in collaboration with cross-functional teams
• Ensure alignment between literature-derived safety data and ICSR records
• Support ongoing pharmacovigilance compliance and inspection readiness

Systems, Training, and Access Management

• Support training documentation related to literature surveillance processes
• Manage user access and roles in literature surveillance and reconciliation databases
• Maintain system documentation in line with internal SOPs and regulatory expectations

Communication and Coordination

• Manage and monitor team mailboxes to ensure timely action on incoming requests
• Coordinate with global stakeholders and functional teams to resolve safety-related queries
• Support smooth information flow within matrix teams operating across regions

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Eligibility / Qualifications

Educational Qualification

Candidates must hold a medical or scientific degree.

Relevant courses include: MBBS, BPharm, MPharm, PharmD, MSc Life Sciences, MSc Pharmacology, MSc Clinical Research, PhD Life Sciences

Experience Requirements

• Minimum 3 years of experience in a pharmacovigilance or patient safety environment
• Prior experience in literature safety surveillance and ICSR reconciliation is highly preferred
• Hands-on exposure to global drug safety regulations for development and post-authorization products
• Experience working with safety databases; exposure to ArisG safety database is an advantage

Key Skills and Knowledge

• Strong understanding of global pharmacovigilance regulations and guidelines
• Knowledge of drug safety requirements for clinical and post-marketing products
• Excellent written and verbal communication skills
• Experience working in international and cross-cultural team environments
• Strong attention to detail and quality-focused mindset

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Location & Salary

• Job Location: Bangalore, Karnataka
• Employment Type: Full-time
• Work Model: Office-based / hybrid as per business requirements
• Salary: Competitive and aligned with industry standards for pharmacovigilance analyst roles

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Application Process

Interested candidates can apply through the official Merck career portal using the link below:

Apply here: https://careers.merckgroup.com/global/en/job/294925/Literature-Surveillance-and-Reconciliation-Analyst

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FAQs – Literature Surveillance and Reconciliation Analyst

Who can apply for this role?

Candidates with a medical or scientific degree and at least 3 years of pharmacovigilance experience can apply.

Is this role suitable for freshers?

No. Prior experience in literature surveillance or ICSR reconciliation is required.

Does the 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 teams in a matrix environment.

What are the career growth opportunities?

This role offers growth into senior patient safety, signal management, and global pharmacovigilance leadership positions.

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Summary Table

Company	Merck
Vacancies	Literature Surveillance and Reconciliation Analyst
Required Education	Medical / Scientific Degree (Pharmacy, Life Sciences, Medicine)
Experience	3+ years in Pharmacovigilance / Patient Safety

Tagged as: Pharma Jobs in Bangalore