Senior Pharmacovigilance Associate at ICON will lead the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting according to regulatory guidelines
Job Summary
Senior Pharmacovigilance Associate at ICON will lead the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting according to regulatory guidelines.
ICON offers a diverse and inclusive culture with competitive salary and benefits focused on well-being and work-life balance for employees and their families.
The role requires collaboration with medical and clinical teams, engagement in audits and inspections, and staying informed on evolving regulatory guidelines to enhance pharmacovigilance processes.
Matching Summary
Senior Pharmacovigilance Associate at ICON will lead the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting according to regulatory guidelines.
Skills & Requirements
Must-have
Pharmacovigilance process management
Adverse event reporting
Regulatory compliance in pharmacovigilance
Pharmacovigilance databases proficiency
Data analysis of safety data
Hybrid work arrangement
Nice-to-have
Training and mentoring skills
Cross-functional team collaboration
Knowledge of MedDRA coding
Strong communication skills
Critical thinking and analytical skills
Key Requirements
Bachelor’s degree in life sciences or related field
Extensive pharmacovigilance or drug safety experience