Novotech hiring Pharmacovigilance Associate in Bangalore. Apply for PV job with ICSR processing, safety database and ICH GCP compliance experience.
Introduction
Pharmacovigilance professionals aiming to grow in drug safety and clinical research can explore this excellent opportunity. Novotech is hiring a Pharmacovigilance Associate in Bangalore. This role offers hands-on exposure to safety case processing, regulatory compliance, and clinical trial pharmacovigilance activities.
Company Overview
Novotech is a globally recognized contract research organization (CRO) providing clinical development services to pharmaceutical and biotech companies. With a strong presence across Asia-Pacific and international markets, Novotech specializes in clinical trials, regulatory compliance, and data-driven research solutions.
Job Location & Employment Type
- Location: Bangalore, Karnataka, India
- Workplace: Helios Business Park
- Job Type: Full-Time
- Industry: Pharmacovigilance / Drug Safety / Clinical Research
Job Overview (Job Details Table)
| Job Title | Pharmacovigilance Associate |
|---|---|
| Company Name | Novotech |
| Qualification | Life Sciences / Pharmacy / Related Field |
| Experience | Relevant experience preferred |
| Job Location | Bangalore, Karnataka |
| Employment Type | Full-Time |
| Salary | As per company norms |
| Application Mode | Online Application |
| Department | Pharmacovigilance / Drug Safety |
| Job ID | 3832 |
Open Positions / Department Details
The role is part of the Pharmacovigilance (Drug Safety) Department, focusing on safety monitoring, case processing, and regulatory compliance for clinical trials and post-marketing surveillance activities.
Key Roles & Responsibilities
As a Pharmacovigilance Associate, your responsibilities will include:
- Monitoring and managing safety aspects of clinical studies and post-marketing activities
- Handling and monitoring safety mailboxes
- Preparing Safety Management Plans (SMPs)
- Setting up and maintaining safety databases for studies
- Processing and submitting ICSRs including:
- Serious Adverse Events (SAEs)
- Suspected Unexpected Serious Adverse Reactions (SUSARs)
- Adverse Events (AEs)
- Ensuring compliance with:
- ICH-GCP guidelines
- Company SOPs
- Global regulatory requirements
- Maintaining accurate safety documentation and reports
- Supporting audits, inspections, and compliance checks
Eligibility Criteria
Educational Qualification
- Degree in:
- Life Sciences
- Pharmacy
- Biotechnology
- Related discipline
Experience Required
- Relevant experience in pharmacovigilance or drug safety
- Experience in ICSR processing and safety database management is preferred
Skills Required
- Knowledge of pharmacovigilance processes and workflows
- Understanding of ICH-GCP guidelines and regulatory requirements
- Experience in ICSR case processing
- Familiarity with safety databases (Argus, ArisG, etc.) is a plus
- Strong attention to detail and documentation skills
- Good communication and teamwork abilities
- Ability to manage timelines and handle multiple tasks
Salary & Benefits
- Salary: As per company norms
- Opportunity to work in a global CRO environment
- Exposure to international pharmacovigilance practices
- Career growth in drug safety and regulatory compliance
- Professional and collaborative work culture
Selection Process
The recruitment process may include:
- Application Screening
- Technical Interview (Pharmacovigilance Focus)
- HR Discussion
- Final Selection
Candidates with hands-on PV experience and strong regulatory knowledge will have an advantage.
How to Apply
Interested candidates should apply through the official Novotech career portal using the job reference details:
- Job ID: 3832
Ensure your resume highlights:
- Pharmacovigilance experience
- ICSR case processing knowledge
- Safety database exposure
Important Dates
- Last Date to Apply: April 29, 2026
Why Apply for This Pharma Job?
This role is ideal for candidates looking to build or grow their career in pharmacovigilance:
- Work with a global CRO (Novotech)
- Gain expertise in ICSR processing and safety systems
- Exposure to global regulatory requirements
- Opportunity to work on clinical trials and post-marketing safety
- Strong career pathway in drug safety and regulatory affairs
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any company or recruiter. Candidates are advised to verify all details independently before applying. We do not charge any fee for job applications.
Final Call-to-Action
If you have experience in pharmacovigilance and want to grow in a global clinical research environment, apply before the deadline. This Novotech opportunity can help you build a strong career in drug safety and regulatory compliance.
