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Job Description

Pharmacovigilance and Case Intake Specialist

布宜諾斯艾利斯, 阿根廷 R1457145

布宜諾斯艾利斯, 阿根廷| 布兰卡港, 阿根廷| 科尔多瓦, 阿根廷| 科连特斯, 阿根廷| 福莫萨, 阿根廷| 拉里奧哈, 阿根廷| 马德普拉塔, 阿根廷| 门多萨, 阿根廷| 内乌肯, 阿根廷| 巴拉那, 阿根廷| 波萨达斯, 阿根廷| 罗森, 阿根廷| 雷西斯滕西亚, 阿根廷| 里奥加耶戈斯, 阿根廷| 罗萨里奥, 阿根廷| 萨尔塔, 阿根廷| Cuscuden San Fco. Del Monte, 秘鲁| 圣胡安, 阿根廷| 聖路易斯, 阿根廷| 圣米格尔-德图库曼, 阿根廷| 圣萨尔瓦多-德胡胡伊, 阿根廷| Santa Fe, 阿根廷| 圣地亚哥-德尔埃斯特罗, 阿根廷| 乌斯怀亚, 阿根廷| 別德馬, 阿根廷| 阿根廷| Remote

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职位描述

Job Overview

The Pharmacovigilance and Case Intake Specialist/Operations Specialist 1 reviews, assesses, and processes safety data. This role involves distributing reports/data to internal and external parties, following regulations, SOPs, and guidelines with support from senior team members.

Essential Functions

  • Complete assigned training on time.

  • Process safety data per regulations, guidelines, SOPs, and project requirements.

  • Perform pharmacovigilance activities, including:

    • Collecting and tracking Adverse Events (AEs).

    • Determining status of incoming events.

    • Database entry and coding AEs/products.

    • Writing narratives and conducting literature-related activities.

  • Ensure quality and productivity standards are met.

  • Comply with all project-related processes and activities.

  • Read and acknowledge necessary SOPs and ensure timely training.

  • Create, maintain, and track cases.

  • Identify and report quality issues.

  • Demonstrate problem-solving skills.

  • Liaise with team members and healthcare professionals to address project issues.

  • May liaise with clients on case processing activities.

  • Mentor new team members if assigned.

  • Attend project meetings and provide feedback.

  • Perform other duties as assigned.

  • Lead/support department initiatives.

  • Ensure compliance with all people practices and processes.

  • Perform medical review of non-serious AEs and ADRs as required.

Qualifications

  • Bachelor's degree in life sciences

  • Up to 1 year in pharmacovigilance and/or intake case processing

  • Advanced level of English

  • Good knowledge of medical terminology and safety databases.

  • Knowledge of global, regional, and local clinical research regulations.

  • Excellent attention to detail and accuracy.

  • Strong organizational, time management, and communication skills.

  • Self-motivated, flexible, and able to work independently.

  • Ability to multi-task, meet deadlines, and manage competing priorities.

  • Ability to delegate and adapt to changing demands.

  • Willingness to learn new skills across safety service lines.

  • Ability to establish effective working relationships with coworkers, managers, and clients.

  • Team player with a focus on quality deliverables.

  • Demonstration of core values in daily tasks.

  • Extensive use of telephone and face-to-face communication.

  • Regular sitting for extended periods.

  • May require occasional travel and flexibility to operate in shifts.

#LI-Remote

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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