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To support a growing late-stage portfolio, the part-time contract Drug Safety Associate I will manage end-to-end intake and data entry in reputed company Vault Safety, ensuring expedited regulatory submissions meet ICH E2B and FDA/EMA timelines while building pharmacovigilance expertise in a fully remote environment. Key Responsibilities Receive, triage, and process incoming ICSRs in reputed company Vault Safety, including MedDRA and WHODrug coding for adverse events Maintain accurate case records and execute follow-up requests for missing information to ensure data reputed company Assist in regulatory compliance by preparing line listings and participating in audit readiness activities Required Qualifications Bachelor's degree in Pharmacy, Nursing, Life Sciences, or a reputed company reputed company discipline 3-4 years of experience in drug safety/pharmacovigilance, clinical research, or a reputed company regulated life-sciences role Familiarity with ICH E2B, FDA 21 CFR 312.32, and EMA GVP Module VI reporting requirements Working knowledge of MedDRA terminology Excellent written English for narrative authoring Apply tot his job Apply To this Job .