Pharmacovigilance Analyst

Job Summary Join our dynamic team as a Pharmacovigilance Specialist 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 a balanced work environment with no travel required allowing you to make a significant impact from the comfort of your preferred location. Responsibilities Monitor and evaluate adverse event reports to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to analyze and interpret safety data. Assist in the preparation of safety reports and regulatory submissions. Support the development and maintenance of pharmacovigilance systems and processes. Conduct literature reviews to identify potential safety signals. Provide input into risk management plans and safety assessments. Ensure timely and accurate case processing and data entry. Participate in safety review meetings and contribute to decision‑making processes. Maintain up‑to‑date knowledge of pharmacovigilance regulations and guidelines. Assist in the training and mentoring of junior team members. Contribute to the continuous improvement of pharmacovigilance practices. Engage with stakeholders to communicate safety findings and recommendations. Utilize technical skills in Pharma Research & Development to enhance data analysis capabilities. Qualifications Possess a degree in a relevant scientific discipline. Demonstrate experience in Pharma Research & Development. Exhibit strong analytical and problem‑solving skills. Show proficiency in pharmacovigilance data management. Have experience in PV Case Processing as a nice to have skill. Display excellent communication and teamwork abilities. Maintain a keen attention to detail and accuracy. Certifications Required Certification in Pharmacovigilance or Drug Safety Management. #J-18808-Ljbffr