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

• Assist in the monitoring and reporting of safety for pharmaceutical products.

• Take charge of pharmacovigilance and drug safety deliverables, utilizing your expertise to ensure both quality and efficiency.

• Aid in the gathering, examination, and processing of adverse event data in line with pharmacovigilance regulations and company protocols.

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

• Work alongside cross-functional teams to guarantee timely and accurate dissemination of safety information.

• Contribute to the creation and upkeep of pharmacovigilance documentation, including standard operating procedures and safety management plans.

• Engage in training and development initiatives to enhance your understanding of pharmacovigilance practices and regulatory requirements.

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

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

• Strong communication and interpersonal skills, enabling collaborative teamwork.

• A basic 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.

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

• Attractive base salary with performance-related incentives.

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

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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

Graduate Pharmacovigilance Associate

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