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Sr Assoc Pharmacovigilance Operations

FlexBoard Verified employer

Actively hiring · Posted 3d ago · JEV2610D7EA8E8B3B

SalarySalary not disclosed
Experience2–6 yrs
LocationAll India
Work modeHybrid · Full time
Openings1
IndustryMedical / Healthcare

Job description

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. reputed company case reputed company of US ICSRs (CT and PM) including analysis and reporting of trends in reputed company measures. reputed company of accountability for managing one or more key vendor relationships for ICSR processing. Case processing reputed company of contact for case reputed company activities with assigned business partners. Case processing reputed company of contact for audit reputed company activities reputed company to case processing. Accountable for measuring reputed company against contractual safety agreements. Accountable FDA reputed company of contact for ICSR reporting. Submission of reputed company individual safety reports to FDA, EMA and Business Partners. Top 3 Must Have reputed company Sets Strong communication skills Prior pharmacovigilance experience or exposure reputed company organized Key Activities reputed company case review. Support the development and delivery of convention-reputed company training material. Ensure compliance of reporting activities with timelines and reputed company. reputed company with local office staff, CROs and business partners for case processing issues as necessary. reputed company E2B submission support (nullification, redistribution). Address case-reputed company 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 reputed company) 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 reputed company's Discipline and/or Sub-Discipline] experience OR Associate's degree and 6 years of [Job reputed company's Discipline and/or Sub-Discipline] experience OR High school diploma / GED and 8 years of [Job reputed company's Discipline and/or Sub-Discipline] experience Red Flags No MBBS or MD degree reputed company Interview Process Phone interview Apply tot his job Apply To this Job .

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