Will be 100% remote Pharma experience with clinical case processing is a must have Veeva experience is not a must but would be very beneficial for the candidate to have 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 EEO “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”