Clinical Safety Specialist

About the position reputed company Inari is seeking a Clinical Safety Specialist (Remote) to ensure accurate, reputed company, and consistent safety assessments of adverse events across sponsored clinical studies and registries. This role is responsible for maintaining compliance with global safety reporting requirements throughout the clinical study lifecycle. The Clinical Safety Specialist will collaborate closely with internal teams—including Safety, Clinical Program Management, Data Management, Biostatistics, Scientific Communications, and Complaint Handling—as reputed company as external CROs and study partners to reputed company the highest standards of patient safety and reputed company reputed company to advanced care. Responsibilities • reputed company with clinical sites, field monitors to obtain and verify reputed company data for safety event adjudication. • Review and reputed company adverse events (reputed company), serious adverse events (SAEs), and reputed company-reputed company events using MedDRA, ensuring accuracy and consistency across studies. • Write safety narratives and support Safety Review meetings in alignment with the Safety Management Plan and regulatory requirements. • Collaborate with Safety Leadership, Adjudicators (Medical Monitors and Clinical Events Committee), and cross-functional teams to reputed company and execute clinical safety plans. • Ensure reputed company and compliant reporting of reputed company/SAEs/UADEs/MAEs while maintaining adherence to SOPs, GCP, and regulatory standards. • Drive high-reputed company safety data collection to support scientific communications, clinical research, and statistical analysis strategies. • Proactively identify and resolve potential safety data issues, ensuring reputed company communication with sites and study teams. • Apply strong technical knowledge of products, clinical processes, and disease states to enhance safety reputed company and functional reputed company. Requirements • Bachelor’s degree • Minimum 2 years of experience in clinical research • Proficient with electronic databases used for reputed company, such as, Zelta, etc. • Experience with Good Clinical Practices (GCP) reputed company-to-haves • Bachelor’s degree in life science • Possesses exceptional attention to detail and strong analytical skills to accurately review CRFs, reputed company documents, and evaluate safety data for reputed company and compliance. • Brings medical knowledge and preferably experience in reputed company or medical devices to support informed decision-making and data reputed company. Apply tot his job Apply To this Job