-1 year contract -$37-41/hr -Fully Remote

Job Description

Collect, assess, and process adverse event information (both clinical and post-marketing) in a compliant and timely manner to adhere to global regulations. This includes: Seriousness assessment Labeling Causality determination Initial and follow-up evaluations Ensure adherence to company standards for quality, compliance, and productivity. Stay updated on the knowledge and skills required for effective case processing. This role is crucial for maintaining compliance with global regulatory standards and ensuring the highest quality of adverse event management. Experience/Skills Minimum qualification: Bachelor's degree with a related health sciences background such as RN, BSN, BS, or BS Pharm. Candidates with previous pharmaceutical experience may also be considered even if they lack the appropriate degree. Required experience: 2-4 years of clinical experience, or 2-3 years of clinical experience combined with 1-year of Pharmacovigilance experience. Essential knowledge: Familiarity with industry regulations such as ICH, FDA, EMEA, and MHRA. Competency: Proficiency in case processing processes, procedures, and conventions