Pharmacovigilance Associate Jobs at ICON plc Trivandrum for professionals with clinical trial case processing or LSMV database experience.
Job Requisition ID: JR139660
Job Type: Full Time
Work Mode: Office with Flex
Location: Trivandrum, India
Industry: Pharmacovigilance, Clinical Research, Drug Safety
Application Mode: Online Application
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, and medical device companies globally. ICON plays a critical role in shaping the future of clinical development through high-quality research, regulatory compliance, and patient safety.
The organization is committed to fostering an inclusive, diverse, and high-performance culture where innovation, collaboration, and excellence drive meaningful outcomes for patients worldwide. Pharmacovigilance Associate Jobs at ICON plc
Job Details
Job Title: Pharmacovigilance Associate
Company: ICON plc
Location: Trivandrum, India
Work Model: Office with Flex
Employment Type: Full Time
Functional Area: Pharmacovigilance / Drug Safety
Focus Area: Clinical Trial Case Processing / LSMV Database
Job Description
ICON is seeking a Pharmacovigilance Associate to join its dynamic Drug Safety team in Trivandrum. This role is ideal for professionals with at least two years of experience in pharmacovigilance case processing, particularly in clinical trial safety cases or with hands-on experience using the LSMV database. Pharmacovigilance Associate Jobs at ICON plc
The Pharmacovigilance Associate will play a key role in ensuring patient safety by collecting, assessing, processing, and reporting adverse event data in compliance with global regulatory requirements and industry standards. Pharmacovigilance Associate Jobs at ICON plc
Key Responsibilities
- Collect, assess, and process adverse event reports in accordance with regulatory timelines
- Perform pharmacovigilance case processing for clinical trial safety cases
- Utilize and manage safety data within the LSMV database
- Ensure accuracy, completeness, and compliance of safety case documentation
- Support signal detection activities and assist with safety risk assessments
- Collaborate with cross-functional teams to address safety-related queries
- Support ongoing safety investigations and follow-up activities
- Maintain up-to-date knowledge of global pharmacovigilance regulations and guidelines
- Ensure adherence to internal SOPs, regulatory requirements, and quality standards
Pharmacovigilance Associate Jobs at ICON plc
Skills / Qualifications
Educational Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline
- Advanced degree is preferred
Experience Requirements
- Minimum 2+ years of experience in pharmacovigilance case processing
- Direct experience in one of the following is mandatory:
- Clinical Trial safety case processing
- Hands-on experience with LSMV safety database
- Pharmacovigilance Associate Jobs at ICON plc
Required Skills & Competencies
- Strong analytical and data review skills
- High attention to detail and documentation accuracy
- Solid understanding of pharmacovigilance regulations and safety reporting
- Excellent written and verbal communication skills
- Ability to collaborate effectively with global and cross-functional teams
- Commitment to quality, compliance, and patient safety
- Ability to manage multiple cases and priorities efficiently
Pharmacovigilance Associate Jobs at ICON plc
Benefits / Perks
- Competitive salary aligned with industry standards
- Flexible working model supporting work-life balance
- Comprehensive health insurance coverage for employees and families
- Retirement and long-term savings plans
- Global Employee Assistance Program with 24/7 professional support
- Life assurance and country-specific optional benefits
- Access to learning, development, and career growth opportunities
- Inclusive and diverse workplace culture
Pharmacovigilance Associate Jobs at ICON plc
Why You Should Join
- Work with a globally recognized clinical research organization
- Contribute directly to patient safety and drug development
- Gain exposure to global safety systems and regulatory standards
- Be part of a supportive, inclusive, and innovation-driven environment
- Build long-term career growth in pharmacovigilance and drug safety
Pharmacovigilance Associate Jobs at ICON plc
Frequently Asked Questions (FAQs)
Is clinical trial case processing experience mandatory?
Yes, candidates must have experience in clinical trial safety cases or LSMV database handling.
Is this a remote role?
No, this is an office-based role with flexible working options.
Is LSMV experience mandatory?
LSMV experience is required if the candidate does not have clinical trial case processing exposure.
Is this role suitable for mid-level PV professionals?
Yes, the role is designed for professionals with at least two years of PV experience.
How to Apply
Interested and eligible candidates should apply through the official ICON careers portal.
Current ICON employees should apply through the internal careers portal.
Only shortlisted candidates will be contacted for the next stages of the selection process.
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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.
