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"Pharmacovigilance Associate Job at ICON plc – Trivandrum & Chennai | Apply Now"
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"Pharmacovigilance Associate Job at ICON plc – Complete Details."
(Pharmacovigilance Associate Job at ICON plc)
Introduction
Pharmacovigilance has become one of the most critical domains in the pharmaceutical and clinical research industry due to increasing regulatory expectations and a strong focus on patient safety. Global clinical research organizations are constantly hiring experienced professionals who can manage safety data accurately and ensure compliance with international regulations.
ICON plc, a globally recognized clinical research organization, is currently hiring Pharmacovigilance Associates for its Trivandrum (Kerala) and Chennai offices. This opportunity is ideal for professionals with 2+ years of experience in pharmacovigilance case processing, especially those who have worked on clinical trial safety cases or LSMV databases.
About the Company – ICON plc
ICON plc is a leading global healthcare intelligence and clinical research organization providing outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies.
Company Name: ICON plc
Headquarters: Dublin, Ireland
Founded: 1990
Global Presence: 40+ countries
Employees: 40,000+ worldwide
ICON is known for its strong focus on clinical research, drug safety, regulatory compliance, and patient-centered innovation. The company supports clinical development programs across all phases and therapeutic areas.
Job Overview Summary
The Pharmacovigilance Associate role at ICON is a full-time, office-based position focused on clinical trial safety case processing and global drug safety surveillance. The selected candidate will work closely with cross-functional teams to ensure accurate handling of adverse event data and compliance with international pharmacovigilance guidelines.
This role plays a direct role in protecting patient safety and supporting regulatory submissions for global clinical trials.
Vacancy Details (Official)
Job Title: Pharmacovigilance Associate
Job ID: JR139660
Company: ICON plc
Location: Trivandrum, Kerala & Chennai, India
Employment Type: Full-time (Office-based)
Domain: Drug Safety / Pharmacovigilance
Experience Required: Minimum 2 years
Job Role & Responsibility Explanation
As a Pharmacovigilance Associate at ICON, the professional will be responsible for end-to-end management of safety cases related to clinical trials. The role requires strong knowledge of pharmacovigilance processes, regulatory timelines, and safety databases.
Key responsibilities include:
Performing complete case processing for clinical trial safety cases
Reviewing and assessing adverse events (AEs) and serious adverse events (SAEs)
Ensuring accurate and timely data entry into LSMV or similar safety databases
Maintaining compliance with ICH-GCP, GVP, FDA, and EMA regulations
Supporting signal detection and safety risk assessments
Collaborating with global safety, clinical, and regulatory teams
Ensuring data quality, accuracy, and regulatory readiness
Eligibility Criteria (Official)
Educational Qualification
Bachelor’s degree in:
Pharmacy
Life Sciences
Or related discipline
Experience Requirement
Mandatory minimum 2+ years of experience in:
Pharmacovigilance case processing
Clinical trial safety cases
LSMV / Argus / similar safety databases
Skills Required
To succeed in this role, candidates should have:
Strong understanding of pharmacovigilance processes
Hands-on experience in safety database operations
Knowledge of global drug safety regulations
High attention to detail and data accuracy
Strong analytical and problem-solving skills
Good written and verbal communication skills
Ability to work in cross-functional global teams
Salary Estimate
Estimated Salary Range: ₹6,00,000 – ₹10,00,000 per annum (CTC)
The final compensation depends on:
Years of pharmacovigilance experience
Type of safety cases handled
Database expertise and compliance knowledge
ICON is known for offering competitive packages aligned with global CRO standards.
Interview Details (Official)
Interview Process:
Technical pharmacovigilance interview
Database and case processing discussion
HR round
Interview Mode: Online / On-site (as per company decision)
Shortlisted candidates will be contacted directly by ICON’s recruitment team.
Required Documents
Applicants should keep the following documents ready:
Updated CV / Resume
Educational certificates
Experience letters
Government ID proof
Recent photograph
How to Apply
Interested and eligible candidates can apply through the official ICON career portal:
It is recommended to apply early, as shortlisting is done on a rolling basis.
FAQs – ICON Pharmacovigilance Associate Job
Q1. Is this job suitable for freshers?
No, this role requires a minimum of 2 years of pharmacovigilance experience.
Q2. Is this role related to clinical trials or post-marketing cases?
This role mainly focuses on clinical trial safety cases.
Q3. Which safety databases are preferred?
Experience with LSMV, Argus, or similar databases is preferred.
Q4. Is work-from-home available?
No, this is a full-time office-based role.
Final Conclusion
The Pharmacovigilance Associate job at ICON plc is an excellent opportunity for experienced drug safety professionals looking to work with a top global CRO. With exposure to international clinical trials, global regulations, and advanced safety systems, this role offers strong career growth and stability in the pharmacovigilance domain.
Candidates with solid case processing experience and a passion for patient safety should definitely consider applying.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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