Job Title:
Pharmacovigilance Reporting Associate
Employer:
ICON Plc
Location:
Shanghai, China
Salary:
Competitive
Start Date:
12 April 2025
Closing Date:
12 May 2025
Job Type:
Full-Time
Company Overview:
ICON Plc is a world-leading healthcare intelligence and clinical research organization. The company values innovation, excellence, inclusion, and a collaborative work environment. ICON is on a mission to shape the future of clinical development.
Position Summary:
As a Pharmacovigilance Reporting Associate, you will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities. The role ensures compliance with regulatory requirements and supports patient safety and regulatory success.
Key Responsibilities:
Prepare and review safety reports including periodic safety updates and individual case safety reports (ICSRs).
Collect and analyze adverse event data from clinical trials and post-marketing sources.
Maintain current knowledge of pharmacovigilance regulatory requirements and best practices.
Collaborate with clinical, regulatory, and data management teams to resolve reporting issues.
Ensure timely submission of safety reports to sponsors and regulatory authorities.
Candidate Profile:
Bachelor’s degree in Life Sciences, Pharmacy, or a related field.
Experience in pharmacovigilance or drug safety with understanding of regulatory safety reporting processes.
Excellent attention to detail and organizational skills.
Strong communication and collaboration skills.
Ability to manage multiple tasks in a fast-paced, regulated environment.
What ICON Offers:
Competitive salary and comprehensive benefits.
Various annual leave entitlements.
Health insurance plans for individuals and families.
Retirement planning support.
Global Employee Assistance Programme (LifeWorks).
Life assurance.
Flexible country-specific optional benefits (e.g., childcare vouchers, bike schemes, gym discounts, travel subsidies).
Diversity & Inclusion:
ICON is committed to providing an inclusive, accessible workplace and encourages all qualified applicants to apply, regardless of background or if all criteria are not met. Reasonable accommodations are available for those who need it.
Application Link:
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