Senior Pharmacovigilance Associate
Location: Mexico (Home-Based – CDMX)
Company: ICON Strategic Solutions
Employment Type: Full-Time
Salary: Competitive
Posted Date: 4 March 2026
Application Deadline: 3 April 2026
About ICON Strategic Solutions
ICON Strategic Solutions, part of ICON plc, is a global leader in healthcare intelligence and clinical research services. The organization partners with pharmaceutical, biotechnology, and medical device companies to accelerate the development of life-saving therapies. With a strong focus on innovation, compliance, and patient safety, ICON provides a collaborative environment where professionals contribute to advancing global clinical development.
ICON is currently seeking an experienced Senior Pharmacovigilance Associate to join its remote team based in Mexico City (CDMX). This role plays a critical part in ensuring the safety monitoring of pharmaceutical products through effective pharmacovigilance practices, regulatory compliance, and safety data analysis.
Experience Required
Candidates should typically have 4–7 years of relevant experience in pharmacovigilance, drug safety, or clinical safety operations within the pharmaceutical, biotechnology, or CRO industry.
Key Responsibilities
Lead the collection, evaluation, and processing of adverse event reports, ensuring accurate and timely reporting in accordance with global regulatory guidelines and company procedures.
Perform detailed analysis and interpretation of safety data to identify trends, risks, and potential safety signals requiring further investigation.
Prepare and submit periodic safety update reports (PSURs) and other pharmacovigilance regulatory documents in compliance with international regulatory requirements.
Collaborate with medical, regulatory, and clinical teams to assess the clinical significance of adverse events and support risk management activities.
Maintain pharmacovigilance databases and ensure the integrity, accuracy, and regulatory compliance of safety data records.
Provide guidance, training, and mentorship to junior pharmacovigilance staff on safety reporting procedures and regulatory expectations.
Support internal and external audits or inspections conducted by regulatory authorities, ensuring readiness and adherence to pharmacovigilance standards.
Stay updated with evolving pharmacovigilance regulations, guidelines, and industry best practices to enhance safety monitoring processes.
Required Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related healthcare discipline.
Advanced degree (Master’s or equivalent) is preferred.
Strong experience in pharmacovigilance operations, including adverse event reporting and safety data management.
Good understanding of international pharmacovigilance regulations and drug safety standards.
Proven ability to interpret complex safety data and contribute to signal detection and risk assessment activities.
Proficiency with pharmacovigilance databases and safety management systems.
Strong analytical, organizational, and problem-solving skills.
Excellent communication and collaboration abilities for cross-functional teamwork.
Ability to manage multiple priorities in a fast-paced global environment while maintaining data confidentiality.
Why Join ICON Strategic Solutions
ICON values high-performing professionals and promotes a diverse and inclusive work environment. Employees benefit from opportunities for career growth while contributing to meaningful work that impacts global healthcare.
Employee Benefits
Competitive compensation package
Generous annual leave and paid time off
Comprehensive health insurance options for employees and families
Retirement planning and savings programs
Global Employee Assistance Programme (LifeWorks) with 24/7 professional support
Life insurance coverage
Flexible country-specific benefits such as childcare support, wellness programs, gym membership discounts, and subsidized travel options
ICON is committed to creating an inclusive workplace that values diversity and equal opportunity. All qualified applicants will be considered for employment without discrimination based on race, gender, religion, sexual orientation, disability, or veteran status.
Professionals interested in advancing their pharmacovigilance careers within a globally recognized clinical research organization are encouraged to apply.
Uttar Pradesh :
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Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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King Abdullah Economic City | Riyadh | Jeddah | Najran | Rabigh | Khulais |Kuala Lumpur :
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Kyiv |Lima Region :
Lima |France :
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