🛡️ Advance Patient Safety as Senior Pharmacovigilance Associate
Join ICON plc as a Senior Pharmacovigilance Associate and leverage your LSMV database expertise to protect patient safety worldwide. This critical role offers the opportunity to lead pharmacovigilance activities while mentoring the next generation of drug safety professionals in a global clinical research environment.
🎯 Your Impact: Key Responsibilities
Case Processing Excellence & LSMV Expertise
- Leverage 4+ years of case processing experience with strong LSMV database skills to manage adverse event reporting
- Lead collection, evaluation, and processing of adverse event reports, ensuring accuracy and timely regulatory submissions
- Maintain and ensure integrity of pharmacovigilance databases while upholding documentation quality standards
- Analyze complex safety data, interpret findings, and identify emerging trends or potential safety issues
Regulatory Compliance & Reporting
- Prepare and submit detailed periodic safety update reports (PSURs) and other regulatory documents
- Ensure compliance with international pharmacovigilance regulations and company standards
- Participate in regulatory audits and inspections, maintaining readiness and full compliance
- Stay current with evolving global regulations and industry advancements in drug safety
Clinical Collaboration & Risk Management
- Work closely with medical and clinical teams to assess clinical importance of reported adverse events
- Support risk management initiatives and contribute to safety surveillance strategies
- Provide expert input on safety data interpretation and clinical implications
- Collaborate with cross-functional teams to ensure comprehensive safety monitoring
Team Leadership & Mentorship
- Train and mentor junior pharmacovigilance staff in procedures, regulations, and best practices
- Share LSMV database expertise and case processing knowledge with team members
- Contribute to continuous improvement of pharmacovigilance processes and training programs
- Foster a culture of excellence and compliance within the drug safety team
⭐ Your Profile: Qualifications & Experience
Essential Requirements
- Bachelor's degree in life sciences, pharmacy, nursing, or related field (advanced degree preferred)
- Minimum 4+ years in pharmacovigilance case processing with demonstrated LSMV database skills
- Extensive experience in pharmacovigilance or drug safety with strong regulatory knowledge
- Proven ability to manage complete pharmacovigilance process including adverse event reporting
Technical Competencies
- Proficiency in pharmacovigilance databases and data management systems
- Strong LSMV database skills with ability to process complex safety cases
- Expertise in Microsoft Office Suite for documentation and reporting
- Understanding of signal detection methodologies and risk management principles
Analytical Capabilities
- Strong analytical and critical thinking skills for complex data interpretation
- Ability to identify safety trends and make informed recommendations
- Attention to detail in case processing and regulatory reporting
- Capacity to handle multiple priorities in fast-paced environment
Professional Attributes
- Excellent communication and interpersonal skills for cross-functional collaboration
- Ability to work independently while contributing to team success
- Commitment to confidentiality and ethical handling of patient information
- Proactive approach to staying current with regulatory changes
💫 Why Join ICON Pharmacovigilance?
Patient Safety Impact
- Play crucial role in ensuring safety and efficacy of pharmaceutical products worldwide
- Protect patient welfare through meticulous adverse event monitoring and reporting
- Contribute to drug safety decisions that impact global healthcare outcomes
- Work at the forefront of pharmacovigilance in leading clinical research organization
Professional Growth
- Clear pathway to Pharmacovigilance Team Lead and Management roles
- Opportunity to mentor junior staff and develop leadership capabilities
- Exposure to diverse therapeutic areas and global safety regulations
- Access to advanced pharmacovigilance training and certification programs
Technical Advancement
- Work with sophisticated LSMV database systems and safety platforms
- Develop expertise in global pharmacovigilance regulations and reporting requirements
- Participate in implementation of new safety technologies and processes
- Gain experience with cutting-edge signal detection and risk management methodologies
Global Collaboration
- Work with international teams across ICON's worldwide network
- Collaborate with regulatory authorities and global health organizations
- Participate in cross-functional teams with medical, clinical, and regulatory experts
- Contribute to global pharmacovigilance standards and best practices
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
Career Development
- Retirement planning and financial security benefits
- Life assurance coverage
- Professional development funding and training opportunities
- Health and wellness programs
- Flexible work arrangements
✨ Ready to Lead Drug Safety Excellence?
If you're an experienced pharmacovigilance professional with strong LSMV database skills and passion for patient safety, we encourage you to apply. This Senior Pharmacovigilance Associate role offers the perfect opportunity to advance your career while making a meaningful impact on global drug safety and patient protection.
Apply Now & Protect Patient Safety Worldwide!
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 LSMV expertise and patient safety commitment might be exactly what we need at ICON!
