Pharmacovigilance Associate
IQVIA
Mexico City, Mexico
hace 1 hora

A project With great impact at IQVIA!

Job Overview

Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports / data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.

Essential Functions

  • To Prioritize and complete the assigned trainings on time.
  • Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.
  • To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE) / endpoint information
  • determining initial / update status of incoming events
  • database entry
  • coding AE and Products, writing narratives, Literature related activities as per internal / project timelines.
  • Ensure to meet quality standards per project requirements.
  • Ensure to meet productivity and delivery standards per project requirements.
  • To ensure compliance to all project related processes and activities.
  • Creating, maintaining and tracking cases as applicable to the project plan.
  • Identify quality problems, if any, and bring them to the attention of a senior team member.
  • To demonstrate problem solving capabilities.
  • To mentor new teams members, if assigned by the Manager.
  • Attend project team meetings and provide feedback to operations manager on any challenges / issues or successes.
  • 100% compliance towards all people practices and processes
  • Perform other duties as assigned.
  • Qualifications

  • High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences
  • An Individual with a minimum of a Bachelor’s Degree in scientific or healthcare discipline or allied life sciences graduation with 1-1.
  • 5 years of relevant experience.

  • Good knowledge of medical terminology.
  • Working knowledge of applicable Safety Database.
  • Knowledge of applicable global, regional, local clinical research regulatory requirements.
  • Excellent attention to detail and accuracy.
  • Good working knowledge of Microsoft Office and web-based applications.
  • Strong organizational skills and time management skills.
  • Strong verbal / written communication skills.
  • Self-motivated and flexible.
  • Ability to follow instructions / guidelines, utilize initiative and work independently.
  • Ability to multi-task, manage competing priorities and deadlines.
  • Ability to delegate to less experienced team members.
  • Willingness and aptitude to learn new skills across Safety service lines.
  • Ability to establish and maintain effective communication and working relationships with coworkers, managers and clients.
  • Ability to work as a Team Player, contribute and work towards achieving Team goals.
  • Ensure quality of deliverables according to the agreed terms.
  • Demonstration of IQVIA core values while doing daily tasks - Extensive use of keyboard requiring repetitive motion of fingers.
  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
  • Regular sitting for extended periods of time.
  • May require occasional travel.
  • Flexibility to operate in shifts.
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