Clinexa is a Clinical Research Organization (CRO) dedicated to supporting pharmaceutical, biotechnology, and healthcare partners in the successful delivery of clinical trials and research programs. The company fosters a collaborative and fast-paced environment where professionals are empowered to contribute to innovative research, uphold high standards of quality and compliance, and grow their careers within the evolving clinical research and life sciences industry.

Clinexa is seeking a Pharmacovigilance Officer to support drug safety and pharmacovigilance activities across clinical trials and post-marketing programs for pharmaceutical and biotechnology clients. The role is responsible for processing and reviewing adverse event reports, ensuring timely safety reporting in compliance with global regulatory requirements, and supporting safety surveillance activities throughout the product lifecycle.

The successful candidate will work closely with clinical operations, medical, regulatory, and sponsor teams to maintain accurate safety databases, prepare safety documentation, and contribute to signal detection and risk management activities. This position requires strong attention to detail, knowledge of ICH-GCP and global pharmacovigilance regulations, and the ability to work effectively in a fast-paced and collaborative clinical research environment.

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