Pharmacovigilance Supervisor

This is a fully remote position, open to applicants in Mexico.

📋 Description

• Oversee the monitoring and reporting of safety concerning adverse events linked to clinical trials and marketed products.

• Manage the daily activities related to pharmacovigilance and drug safety.

• Supervise pharmacovigilance operations to guarantee timely and precise reporting of adverse events.

• Collaborate with clinical operations and regulatory affairs to enhance pharmacovigilance processes.

• Ensure compliance with global regulatory standards and internal standard operating procedures for safety reporting.

• Manage the collection, analysis, and submission of safety data to regulatory authorities.

• Provide leadership and training to the pharmacovigilance team.

⛳️ Requirements

• A Bachelor's degree in life sciences, pharmacy, or a related discipline.

• Experience in pharmacovigilance or drug safety, particularly in relation to clinical trials or post-marketing surveillance.

• Comprehensive understanding of global pharmacovigilance regulations and guidelines.

• Strong communication, leadership, and organizational skills, with the capability to effectively manage a team.

• Detail-oriented with the ability to handle multiple tasks while ensuring accuracy in safety reporting.

• Legal authorization to work in the country where the position is based.

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

• Health and wellbeing programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Opportunities for learning and development through structured training and career pathways.