Key Facts

Remote From:

Full time

Mid-level (2-5 years)

German, English, Spanish, French

Hard Skills

Adverse Event Monitoring Active Safety Pharmacovigilance Active Safety Regulatory Compliance Endpoint Management Safety Management Systems Clinical Assessments Pharmacovigilance

Other Skills

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Communication
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Time Management
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Teamwork
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Organizational Skills
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Detail Oriented
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Problem Solving

Roles & Responsibilities

Bachelor’s degree in Life sciences or related field
Fluency in English and German or French
Third language proficiency at least B2 with English minimum C1 (to be evaluated)
1 year pharmacovigilance experience valued

Requirements:

Process safety data according to applicable regulations, guidelines, SOPs, and project requirements
Perform pharmacovigilance activities including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status, database entry, coding AEs and products, writing narratives, and literature-related activities
Ensure compliance with quality, productivity, and delivery standards per project requirements
Liaise with different functional team members and healthcare professionals to address project-related issues

IQVIA

Health Care

About IQVIA

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures. To learn more, visit www.iqvia.com.

Company type: Large

Industry: Health Care

Founded: 2018

Company size: 10001

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Job description

Job Overview

Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members. This is a trilingual role requiring fluency in English, Spanish, and German (or) French.

Main Responsibilities

Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.
Ensure compliance with quality, productivity, and delivery standards per project requirements.
Liaise with different functional team members and healthcare professionals to address project-related issues.

Qualifications

Bachelor’s degree in Life sciences or a related field (mandatory)
Fluency in English and German or French (mandatory) We're considering B2 level in third language as long as you can reach a C1 minimum in English! (will be evaluated)
Up to 3 years of previous clinical experience (desirable)
1 year of pharmacovigilance experience will be highly valued (desirable)

What we offer to you:

OSDE 310
Annual bonus by performance
Salary adjustments during the year according to inflation rates.
21 vacations days
Work flexibility
100% remote role!

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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