Pharmacovigilance Analyst
hace 7 días
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.
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