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Pharmacovigilance / PV Manager (m/w/d) – Heidenheim/Berlin/Porto/Riga oder remote

The Force

Role overview

Qualifications

  • Extensive experience in pharmacovigilance and PV systems development, performance monitoring, and regulatory compliance
  • Ability to lead, coordinate, and support PV audits and inspections
  • Strong medical writing skills across the PV lifecycle, with experience in Medical Literature Monitoring, signal management, ICSR management, and SUSAR management
  • Knowledge of quality management systems in pharmacovigilance and management of standard operating procedures (SOPs)

Responsibilities

  • Build and optimize systems and processes to enable clients to perform effective PV activities and monitor the performance and compliance of PV systems
  • Lead, coordinate, and support PV audits and inspections
  • Create PV documentation across product lifecycles through medical writing and manage activities such as Medical Literature Monitoring, signal management, ICSR and SUSAR handling
  • Maintain and manage quality management systems in PV and SOP administration

About the company

The Force logo

The Force

Design Services

Mixing science, tech, and arts, we explore de digital and physical world to create innovative experiences.Based in São Paulo, we connect to an international team of people afficcionated with new ways to present the beauty of the human experience in mesmerizing and unconventional media. Our portfolio includes companies and artists such as Kent, Elle, Heineken, Schultz, Nike, Rosa Chá, Nonotak, Pabllo Vittar, Hoegaarden, Oi, Gaia, Amarello, Bradesco, Jahnkoy, Becks, Alok, Givanchy, Paco Rabanne, Boiler Room, Coca Cola, Mila Magia, Esfér, and others.Colaborate with us in our projects to come sending your resumé to careers@theforce.cc.

Company details

Company typeSME
IndustryDesign Services
Company size51 - 200

Links

Website LinkedIn See all jobs

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Job description

ECKPUNKTE

Wir suchen eine*n
PHARMACOVIGILANCE / PV MANAGER (m/w/d)
Standort: Heidenheim/Berlin/Porto/Riga oder remote (Deutschland/Portugal/Lettland)
Start: zum nächstmöglichen Zeitpunkt

DEINE AUFGABEN

DEINE MISSION:
  • Der Aufbau von Systemen und Prozessen, die es unseren Kunden ermöglichen, effektive PV-Aktivitäten durchzuführen, gehört ebenso zu deiner Mission wie die Überwachung der Performance und Konformität von PV-Systemen.
  • Du leitest, koordinierst und unterstützt PV-Audits und -Inspektionen.
  • Medical Writing gibt dir nicht das Gefühl, von einem anderen Stern zu sein, was es dir ermöglicht, PV-Dokumente über den gesamten Lebenszyklus der Produkte unserer Kunden zu gestalten.
  • Aufgaben wie Medical Literature Monitoring, Signalmanagement, ICSR Management und SUSAR Management sind für dich keine unbekannten Objekte – oder du bist bereit, dich in diesen Sphären weiterzuentwickeln.
  • Du bist mit dem Kosmos von Qualitätsmanagementsystemen in der Pharmakovigilanz und der Verwaltung von Standardarbeitsanweisungen (SOPs) vertraut und kümmerst dich auch um diese.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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