Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Pharmacovigilance Specialist based in India.
This role sits at the core of drug safety operations, ensuring the continuous monitoring, assessment, and documentation of adverse events across clinical trials and post-marketing surveillance. You will play a key role in safeguarding patient safety by ensuring accurate case processing, regulatory compliance, and high-quality safety reporting. The position involves close collaboration with cross-functional teams and global stakeholders in a regulated life sciences environment. You will be responsible for evaluating complex safety data, contributing to regulatory submissions, and ensuring adherence to global pharmacovigilance standards. The role also includes peer review, mentoring junior colleagues, and supporting continuous improvement in case processing workflows. It is a highly detail-oriented and impact-driven position where scientific rigor and compliance excellence are essential. You will contribute directly to the safety and lifecycle management of innovative therapies.
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Pharmacovigilance Specialist based in India.
This role sits at the core of drug safety operations, ensuring the continuous monitoring, assessment, and documentation of adverse events across clinical trials and post-marketing surveillance. You will play a key role in safeguarding patient safety by ensuring accurate case processing, regulatory compliance, and high-quality safety reporting. The position involves close collaboration with cross-functional teams and global stakeholders in a regulated life sciences environment. You will be responsible for evaluating complex safety data, contributing to regulatory submissions, and ensuring adherence to global pharmacovigilance standards. The role also includes peer review, mentoring junior colleagues, and supporting continuous improvement in case processing workflows. It is a highly detail-oriented and impact-driven position where scientific rigor and compliance excellence are essential. You will contribute directly to the safety and lifecycle management of innovative therapies.