All roles

Sr Assoc Pharmacovigilance Operations

Remote · USA Full-time New today

Job Title: Sr Assoc Pharmacovigilance Operations Duration: 6 Months (PTE) Location: 91320, Thousand Oaks, CA Fully Remote - Any timezone Purpose: To support the safety surveillance process for our products by performing follow up activities with patients and HCPs of individual case safety reports. Ensure vendor compliance with approved processes and training requirements. Oversee case quality of US ICSRs (CT and PM) including analysis and reporting of trends in quality measures. Point of accountability for managing one or more key vendor relationships for ICSR processing. Case processing point of contact for case related activities with assigned business partners. Case processing point of contact for audit related activities related to case processing. Accountable for measuring quality against contractual safety agreements. Accountable FDA point of contact for ICSR reporting. Submission of all individual safety reports to FDA, EMA and Business Partners. Top 3 Must Have Skill Sets: Strong communication skills Prior pharmacovigilance experience or exposure Well organized Key Activities: Perform case review. Support the development and delivery of convention-related training material. Ensure compliance of reporting activities with timelines and criteria. Interface with local office staff, CROs and business partners for case processing issues as necessary. Provide E2B submission support (nullification, redistribution). Address case-related queries from Business Partners. Support antibody re-testing coordination (non-LAO tasks for repeat testing). Knowledge and Skills: Understanding of global regulatory requirements for pharmacovigilance. Familiarity with clinical development processes. Case processing experience. Attention to detail. Competence in safety database usage (preferably in Lifesphere Multivigilance by ArisGlobal) and medical coding. Comprehensive English writing skills. Excellent phone conversations skills. Comprehensive knowledge on MS Office applications. Basic Qualifications: Master's degree OR Bachelor's degree and 2 years of [Job Code's Discipline and/or Sub-Discipline] experience OR Associate's degree and 6 years of [Job Code's Discipline and/or Sub-Discipline] experience OR High school diploma / GED and 8 years of [Job Code's Discipline and/or Sub-Discipline] experience Red Flags: No MBBS or MD degree holders Interview Process: Phone interview Apply tot his job Apply To this Job

Related roles

Pharmacovigilance Specialist – Remote

Remote · USA Full-time

Consultant - Pharmacovigilance/Safety Systems Implementation (Remote)

Remote · USA Full-time

Senior Drug Safety Associate, Pharmcoviligence - US - Remote

Remote · USA Full-time

Associate Director, Drug Safety and Pharmacovigilance

Remote · USA Full-time

Drug Safety Specialist

Remote · USA Full-time

Manager, Drug Safety & Pharmacovigilance - Remote

Remote · USA Full-time

Sr Director, Global Pharmacovigilance

Remote · USA Full-time

Pharmacovigilance Coordinator, Case Processing

Remote · USA Full-time

Senior Director, Global Pharmacovigilance (Safety Physician)

Remote · USA Full-time

Drug Safety Analyst – Remote

Remote · USA Full-time

Remote Veteran Client Support Advisor

Remote · USA Full-time

Early Career GIS Analyst

Remote · USA Full-time

Entry-Level Customer Service & Sales Representative – Remote, Flexible Schedule, Mentorship‑Driven Growth, Residual‑Income Focus

Remote · USA Full-time

Senior Electrical Engineer-Federal Engineering & Design Team

Remote · USA Full-time

Video Archive & Editing Intern

Remote · USA Full-time

Supervisor, Financial Clearance Services

Remote · USA Full-time

Experienced Bi-Lingual Spanish Customer Service Representative – Remote Opportunity with arenaflex

Remote · USA Full-time

UI Developer

Remote · USA Full-time

Experienced Customer Service Representative – Remote Work Opportunity with arenaflex

Remote · USA Full-time

Security GRC Manager

Remote · USA Full-time