Graduate Pharmacovigilance Associate

• Support the collection, review, and processing of adverse event data in accordance with pharmacovigilance regulations and company procedures.
• Assist in the preparation and submission of safety reports to regulatory authorities and stakeholders.
• Collaborate with cross-functional teams to ensure timely and accurate communication of safety information.
• Contribute to the development and maintenance of pharmacovigilance documentation, including standard operating procedures and safety management plans.
• Participate in training and development activities to gain a deeper understanding of pharmacovigilance practices and regulatory requirements.
• Work in a sponsor-dedicated model supported by ICON’s global expertise.

• Bachelor's degree in pharmacy, life sciences, or a related field.
• Strong attention to detail and organizational skills, with the ability to manage multiple tasks and prioritize effectively.
• Excellent communication and interpersonal skills, with the ability to work collaboratively in a team environment.
• Basic understanding of pharmacovigilance principles and regulatory guidelines is desirable but not required; relevant training will be provided.
• Proficiency in Microsoft Office applications, with good analytical and problem-solving skills.
• Willingness to travel as required (approximately 10%).
• Legal right to work in the country where the role is based.

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways