Safety & Pharmacovigilance Associate - 171898

Responsibilities: of the S & P Associate include: • Manage and process Serious Adverse Events (SAEs) in accordance with project-specific requirements. • Maintain and organize safety documentation, electronic files, and tracking systems while supporting document control activities. • Track and process pharmaceutical and Data Management Center (DMC) queries and generate requested safety data reports. • Process safety narratives, assist with MedDRA coding activities, perform quality control reviews on AE submissions, and distribute safety information as required. Qualifications: for the S & P Associate include: • Bachelor's degree with at least 1+ years of clinical research or safety experience, or a scientific/health-related Master's degree with relevant internship experience. • 1+ years of experience in a clinical research environment or bioethics setting. • Knowledge of medical terminology and familiarity with medical research data, experimental protocol review, safety data summarization, and the drug/vaccine development process or clinical trials. Compensation: for S & P Associate includes: • Rate Range: $25-$29/ hr, depending on experience • Comprehensive Benefit Package: Cigna Medical/Dental/Vision, 401K, Sick Leave as Required by Law This job is open for applications on August 12th, 2026. Applications will be accepted at least 30 days from the posting date.