What You Will Do
You will take responsibility for pharmacovigilance and drug safety deliverables, applying your skills to ensure quality and efficiency.
Key Responsibilities Include
- Supporting the collection, review, and processing of adverse event data in accordance with pharmacovigilance regulations and company procedures.
- Assisting in the preparation and submission of safety reports to regulatory authorities and stakeholders.
- Collaborating with cross-functional teams to ensure timely and accurate communication of safety information.
- Contributing to the development and maintenance of pharmacovigilance documentation, including standard operating procedures and safety management plans.
- Participating in training and development activities to gain a deeper understanding of pharmacovigilance practices and regulatory requirements.
Your Profile
You will bring relevant pharmacovigilance and drug safety experience, along with the following qualifications and skills.
Required Qualifications And Experience
- 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%)
What ICON Can Offer You
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-be