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

📋 Description

• Assist in the gathering, evaluation, and processing of adverse event information in compliance with pharmacovigilance regulations and company protocols.

• Aid in the preparation and submission of safety reports to regulatory bodies and stakeholders.

• Work in collaboration with cross-functional teams to ensure timely and precise communication of safety data.

• Support the creation and upkeep of pharmacovigilance documentation, which includes standard operating procedures and safety management plans.

• Engage in training and development opportunities to enhance understanding of pharmacovigilance practices and regulatory standards.

• Assume responsibility for pharmacovigilance and drug safety outputs, utilizing skills to guarantee quality and efficiency.

⛳️ Requirements

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

• Exceptional attention to detail and organizational abilities, with the capacity to handle multiple tasks and prioritize effectively.

• Strong communication and interpersonal skills, with the ability to collaborate effectively within a team setting.

• A foundational understanding of pharmacovigilance principles and regulatory guidelines is preferred but not mandatory; relevant training will be provided.

• Proficiency in Microsoft Office applications, along with strong analytical and problem-solving abilities.

• Willingness to travel as necessary (approximately 10%).

• Employment with ICON is contingent upon possessing the legal right to work in the country where the position is located.