🛡️ Advance Patient Safety as Pharmacovigilance Associate
Join ICON plc as a Pharmacovigilance Associate and leverage your clinical trial case processing or LSMV database expertise to protect patient safety worldwide. This vital role offers the opportunity to develop your drug safety career while ensuring compliance and contributing to meaningful pharmacovigilance operations.
🎯 Your Impact: Key Responsibilities
Case Processing Excellence
- Collect, assess, and process adverse event reports with precision and attention to detail
- Utilize LSMV database skills to manage safety data and ensure accurate case processing
- Handle clinical trial cases efficiently, maintaining compliance with regulatory timelines
- Ensure all adverse event reporting meets global regulatory requirements and company standards
Safety Monitoring & Analysis
- Conduct signal detection activities and support comprehensive risk assessments
- Analyze safety data to identify and evaluate potential safety concerns
- Maintain meticulous documentation of all pharmacovigilance activities
- Support ongoing safety investigations and contribute to risk management strategies
Cross-Functional Collaboration
- Partner with clinical, medical, and regulatory teams to address safety-related inquiries
- Collaborate with global pharmacovigilance colleagues on complex case processing
- Support internal and external stakeholders with safety data and reporting requirements
- Participate in team meetings and contribute to process improvement initiatives
Regulatory Compliance & Knowledge
- Maintain current knowledge of global pharmacovigilance regulations and guidelines
- Ensure adherence to ICH-GCP, FDA, EMA, and other relevant regulatory requirements
- Support audit readiness through accurate documentation and compliance with SOPs
- Stay updated on industry best practices and emerging safety regulations
⭐ Your Profile: Qualifications & Experience
Essential Requirements
- Bachelor's degree in Life Sciences, Pharmacy, or related field
- Minimum 2+ years in pharmacovigilance case processing
- Hands-on experience with either:
- Clinical Trial case processing OR
- LSMV database skills
- Strong analytical capabilities with exceptional attention to detail
Technical Competencies
- Experience with safety database systems (LSMV or similar platforms)
- Understanding of clinical trial safety reporting requirements
- Knowledge of medical terminology and drug safety principles
- Proficiency in documentation and case processing workflows
Professional Attributes
- Excellent communication and interpersonal skills
- Ability to collaborate effectively with cross-functional teams
- Strong commitment to quality and compliance standards
- Adaptability to changing regulatory requirements and priorities
Regulatory Knowledge
- Understanding of global pharmacovigilance regulations
- Familiarity with safety reporting timelines and requirements
- Awareness of ICH guidelines and Good Pharmacovigilance Practices
- Interest in developing expertise in drug safety and risk management
💫 Why Join ICON Pharmacovigilance?
Patient Safety Impact
- Play crucial role in protecting patient safety worldwide
- Contribute to the safe use of pharmaceutical products
- Support development of innovative treatments through robust safety monitoring
- Make meaningful impact on public health and drug safety
Career Development
- Clear pathway to Senior PV Associate and Safety Scientist roles
- Comprehensive training in global pharmacovigilance regulations
- Opportunities for professional certification in drug safety
- Exposure to diverse therapeutic areas and product types
Technical Skill Enhancement
- Develop advanced LSMV database expertise
- Learn cutting-edge safety monitoring methodologies
- Gain experience with global safety reporting requirements
- Access to ICON's global pharmacovigilance training resources
Global Collaboration
- Work with international pharmacovigilance teams
- Participate in global safety surveillance activities
- Collaborate with colleagues across different regions and time zones
- Contribute to worldwide patient safety initiatives
Comprehensive Benefits
- Competitive salary package with performance incentives
- Comprehensive health insurance for you and your family
- Global Employee Assistance Programme with 24/7 support
- Generous annual leave and work-life balance initiatives
Professional Growth
- Retirement planning and financial security benefits
- Life assurance coverage
- Professional development funding and training opportunities
- Health and wellness programs
- Flexible work arrangements
✨ Ready to Launch Your Pharmacovigilance Career?
If you're a detail-oriented professional with pharmacovigilance case processing experience and passion for patient safety, we encourage you to apply. This Pharmacovigilance Associate role offers the perfect opportunity to grow your expertise while contributing to essential drug safety activities that protect patients globally.
Apply Now & Protect Patient Safety Through Excellence!
ICON is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
We welcome applications from all qualified pharmacovigilance professionals - your case processing expertise and commitment to patient safety might be exactly what we need at ICON!
