Pharmacovigilance Job at ICON | Apply NowÂ
Pharmacovigilance job opportunities are growing globally, and ICON plc is now hiring a Pharmacovigilance Reporting Associate in Tbilisi, Georgia. This role is ideal for life science professionals looking to build a strong career in drug safety, regulatory compliance, and clinical research within a leading global organization.
- Job Position: Pharmacovigilance Reporting Associate
- Location: Tbilisi, Georgia (Hybrid)
- Job ID: JR149838
About the Company
Pharmacovigilance job opportunities at ICON Careers offer a chance to work with a world-leading healthcare intelligence and clinical research organization. ICON plc is known for driving innovation and excellence in clinical development while fostering an inclusive and diverse work environment.
Job Description
Pharmacovigilance job roles at ICON Careers involve ensuring accurate and timely preparation of safety reports for clinical trials and post-marketing activities. As a Pharmacovigilance Reporting Associate, you will play a key role in drug safety operations and regulatory compliance within a fast-paced life science job environment.
Qualifications
Pharmacovigilance job eligibility requires:
- Bachelor’s degree in life sciences or a related field
- Experience in pharmacovigilance or drug safety
- Strong understanding of safety reporting processes and regulatory requirements
- Excellent attention to detail and organizational skills
- Strong communication and teamwork abilities
- Ability to manage multiple tasks in a regulated environment
- Willingness to travel (approximately 10%)
Benefits
Job benefits at ICON Careers are designed to support employee well-being and career growth:
- Competitive salary packages
- Annual leave entitlements
- Health insurance options for employees and families
- Retirement planning benefits
- Employee Assistance Programme (LifeWorks)
- Life assurance coverage
- Flexible benefits including childcare vouchers, gym memberships, and travel support
Key Responsibilities
Pharmacovigilance job responsibilities in this life science job include:
- Preparing and reviewing safety reports such as periodic safety updates and individual case safety reports
- Collecting and analyzing adverse event data from clinical trials and post-marketing sources
- Ensuring compliance with global regulatory standards and reporting requirements
- Collaborating with clinical, regulatory, and data management teams
- Managing timely submission of safety reports to regulatory authorities and sponsors
- Staying updated with pharmacovigilance regulations and best practices
