Experience: Not disclosed
Salary: Not disclosed
Location: Not specified
About Us: Join ICON, where diverse teams empower us to advance patients’ lives through drug development.
Role Overview:
As a Senior Pharmacovigilance Reporting Associate, you’ll ensure timely and accurate safety reporting to stakeholders.
Key Responsibilities:
| Responsibility | Qualifications/Experience |
|---|---|
| Submit SAE reports, periodic reports, line listings within project timelines | Bachelor’s degree in relevant field |
| Maintain understanding of safety reporting systems and SOPs | Experience in pharmacovigilance |
| Provide oversight to ensure compliance with regulatory requirements | |
| Collaborate with project team members, clients, investigators, vendors | |
| Maintain databases, prepare for audits and inspections | |
| Mentor junior associates, participate in meetings | |
| Maintain understanding of therapeutic areas |
Benefits:
- Competitive salary packages
- Annual bonuses based on performance
- Health benefits for employees and families
- Retirement plans and life assurance
- Professional growth opportunities
Equal Opportunity Employer: ICON is committed to a discrimination-free workplace.
How to Apply: Apply through the provided link.