Pharmacovigilance Associate Job Clinical Trial Cases LSMV Database skills, and global safety exposure.
Location: Trivandrum, India
Job Reference ID: JR139660
Employment Type: Full-Time, Office-Based
Functional Area: Drug Safety / Pharmacovigilance
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization. ICON partners with pharmaceutical, biotechnology, and medical device companies to advance clinical development and improve patient outcomes worldwide. Pharmacovigilance Associate Job Clinical Trial Cases LSMV Database
The organization is known for its strong commitment to innovation, regulatory excellence, patient safety, and inclusion. ICON fosters a collaborative work environment where employees are encouraged to grow professionally while contributing to meaningful healthcare advancements.
Job Details
ICON is currently hiring a Pharmacovigilance Associate to join its Drug Safety team in Trivandrum. This role is ideal for professionals with hands-on experience in clinical trial case processing or LSMV database operations who are looking to expand their career within a global CRO environment. Pharmacovigilance Associate Job Clinical Trial Cases LSMV Database
Job Description
As a Pharmacovigilance Associate, you will play a critical role in ensuring the safety of investigational and marketed pharmaceutical products. You will be responsible for the accurate collection, assessment, processing, and reporting of adverse event data in compliance with global regulatory requirements. Pharmacovigilance Associate Job Clinical Trial Cases LSMV Database
This position requires strong attention to detail, sound knowledge of pharmacovigilance regulations, and the ability to work cross-functionally with internal and external stakeholders. Pharmacovigilance Associate Job Clinical Trial Cases LSMV Database
Key Responsibilities
- Collect, review, and process adverse event reports from clinical trials in accordance with regulatory timelines
- Perform end-to-end case processing activities, including data entry, narrative writing, and quality review
- Utilize and manage safety data within the LSMV database accurately and efficiently
- Support signal detection activities and assist with safety evaluations and risk assessments
- Collaborate with cross-functional teams to resolve safety queries and support ongoing investigations
- Ensure compliance with global pharmacovigilance regulations, SOPs, and industry guidelines
- Maintain up-to-date knowledge of evolving safety regulations and best practices
Pharmacovigilance Associate Job Clinical Trial Cases LSMV Database
Skills / Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline (advanced degree preferred)
- Minimum 2 years of experience in pharmacovigilance case processing
- Hands-on experience with Clinical Trial safety cases and/or LSMV database
- Strong analytical and data review skills with excellent attention to detail
- Good written and verbal communication skills
- Ability to work effectively in a regulated, deadline-driven environment
- Strong commitment to quality, compliance, and patient safety
Pharmacovigilance Associate Job Clinical Trial Cases LSMV Database
Benefits / Perks
ICON offers a competitive and comprehensive benefits package designed to support employee well-being and work-life balance, including: Pharmacovigilance Associate Job Clinical Trial Cases LSMV Database
- Competitive salary structure
- Multiple annual leave options
- Health insurance plans for employees and eligible dependents
- Retirement and long-term savings plans
- Global Employee Assistance Program (LifeWorks) with 24/7 professional support
- Life assurance coverage
- Country-specific flexible benefits such as childcare support, gym memberships, travel subsidies, and health assessments
Why You Should Join
- Work with a globally recognized clinical research organization
- Gain exposure to international pharmacovigilance standards and processes
- Be part of a diverse, inclusive, and collaborative work culture
- Contribute directly to patient safety and global drug development
- Access continuous learning and career growth opportunities within ICON
Pharmacovigilance Associate Job Clinical Trial Cases LSMV Database
FAQs
Is this role suitable for freshers?
No. This position requires a minimum of 2 years of experience in pharmacovigilance case processing.
Is experience in clinical trials mandatory?
Experience in clinical trial case processing or strong LSMV database skills is required.
Is this an office-based role?
Yes, this is an office-based position in Trivandrum.
Does ICON promote internal career growth?
Yes. ICON strongly supports internal mobility and long-term career development.
How to Apply
For verified pharma job updates, visit PharmaJobHub.in – India’s trusted pharma career portal.
Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
