Pharmacovigilance Associate Job at ICON – Pharma Graduates Apply Now
ICON plc, a global leader in healthcare intelligence and clinical research, is hiring a Pharmacovigilance Reporting Associate for its Chennai office. This full-time opportunity is ideal for professionals experienced in SAE and safety data reporting who want to contribute to high-impact projects in clinical development. Join ICON’s inclusive and innovative work culture and help shape the future of pharmacovigilance.
About ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment that drives innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Job Title: Pharmacovigilance Reporting Associate
Office: India, Chennai
Type: Full-time
Job Requisition ID: JR132021
Job Description
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Submit expedited SAE reports, periodic reports, line listings, and safety data to clients, regulatory authorities, ethics committees, investigators, vendors, and ICON personnel, per project timelines and client agreements.
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Release safety reporting intelligence as per regulatory and internal requirements.
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Maintain a thorough understanding of ICON’s safety reporting systems, SOPs, working procedures, and guidance documents.
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Oversee assigned projects to ensure timely and compliant safety reporting and intelligence releases.
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Act as lead for safety reporting activities, ensuring accountability and adherence to ICON standards and regulatory obligations.
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Support departmental operations, including quality metrics, financial tracking, resource allocation, client engagement, training, and CAPA management.
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Collaborate with internal teams, clients, investigators, and vendors, building effective cross-functional relationships.
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Manage and update project and pharmacovigilance intelligence databases.
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Ensure proper documentation and quality control in eTMF or designated filing systems for audit readiness.
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Represent the department in audits, inspections, and client meetings.
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Stay current on safety regulations and reporting practices; guide and mentor junior staff as needed.
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Support routine project activities including stakeholder communications, metrics review, and budget oversight.
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Maintain therapeutic area knowledge relevant to assigned projects.
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Travel up to 10% domestically/internationally as needed.
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Perform other duties as assigned by management.
Key Responsibilities
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- Oversight of assigned projects to meet safety reporting requirements.
- Collaborate with project team members, clients, and other stakeholders.
Benefits
At ICON, we offer competitive salaries and a range of benefits including various annual leave entitlements, health insurance, retirement planning, and more. Visit our careers site for more details on the benefits we provide.
If you are interested in this role, please apply through the link below:
Keywords: Pharmacovigilance Reporting, Pharmacovigilance Reporting Associate, ICON plc, Healthcare, Clinical Research, Chennai, Job Opening
