PE-Pharmacovigilance

Job Summary

Join our dynamic team as a Pharmacovigilance Associate where you will play a crucial role in ensuring the safety and efficacy of pharmaceutical products. With a focus on Pharma Research & Development you will contribute to the monitoring and evaluation of drug safety data. This hybrid role offers the flexibility of rotational shifts providing a comprehensive experience in the field.

Responsibilities

• Monitor and evaluate adverse event data to ensure drug safety and compliance with regulatory standards.
• Collaborate with cross-functional teams to support the development and implementation of safety monitoring plans.
• Assist in the preparation and submission of safety reports to regulatory authorities.
• Conduct thorough research and analysis of safety data to identify potential risks and trends.
• Support the development of risk management strategies to mitigate identified risks.
• Participate in the review and assessment of safety information from clinical trials and post-marketing sources.
• Provide input and support for the development of safety-related documents and reports.
• Maintain accurate and up-to-date records of safety data and case processing activities.
• Ensure compliance with standard operating procedures and regulatory requirements.
• Contribute to the continuous improvement of pharmacovigilance processes and systems.
• Collaborate with team members to ensure timely and accurate case processing.
• Engage in ongoing training and development to stay current with industry best practices.
• Support the implementation of new pharmacovigilance tools and technologies. Qualifications
• Possess a degree in a relevant scientific field such as pharmacy or life sciences.
• Demonstrate strong analytical and problem-solving skills with attention to detail.
• Exhibit excellent communication and interpersonal skills for effective collaboration.
• Show proficiency in using pharmacovigilance databases and software.
• Have a basic understanding of regulatory requirements and guidelines.
• Display a keen interest in drug safety and pharmacovigilance practices.
• Experience in PV Case Processing is a plus.