Clinical Safety Associate Full-time Job

The Clinical Safety Associate supports clinical trials by monitoring and managing safety data, including adverse drug reactions (ADRs) and other safety-related events. This role involves reviewing and processing safety reports, coordinating with clinical research teams to ensure accurate and timely data reporting, and assisting with the preparation of safety reports and regulatory submissions. The associate is responsible for maintaining safety databases, tracking safety metrics, and contributing to risk management activities. The role requires a thorough understanding of clinical trial processes, pharmacovigilance regulations, and safety reporting requirements. Attention to detail, strong organizational skills, and the ability to work independently are crucial. Experience with safety databases and reporting tools is preferred. Effective communication skills are necessary for interacting with clinical teams, regulatory authorities, and other stakeholders. A degree in life sciences or a related field is required, with prior experience in clinical safety or pharmacovigilance preferred. The role may involve participating in training and development activities to stay current with regulatory changes and industry best practices.