16 Jobs für Pharmacovigilance Specialist
Stellenangebote Pharmacovigilance Specialist Jobs
Job vor 3 Tagen bei Jobleads gefunden
• Ingelheim am Rhein, Rheinland- Pfalz
Homeoffice möglich
Flexible Arbeitszeiten Betriebliche Altersvorsorge Weihnachtsgeld 30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] der zugewiesenen Arzneimittel für das Management sowie Empfehlung von Pharmakovigilanz und Risikomanagement Aktivitäten an Entscheidungsgremien und an die EU QPPV Für wen suchen wir Wir suchen einen [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Patient Safety Physician/ Pharmacovigilance Specialist für ein international agierendes Industrieunternehmen in Ingelheim, zu Beginn ab 01.07.2026. Die Anforderungen Medizinischer Hintergrund: Sie sind approbierter Arzt (m/w/d) und verfügen über fundierte medizinische Kenntnisse. Pharmakovigilanz Kenntnisse: Sie haben ein tiefgehendes Verständnis der Pharmakovigilanz Prozesse und regulatorischen Anforderungen in den wichtigsten Märkten (z. B. EU, [. .. ]
Job vor 8 Tagen bei Neuvoo gefunden
Office Events Wiesbaden
• Ingelheim am Rhein, Rhineland- Palatinate
Homeoffice möglich
Flexible Arbeitszeiten Betriebliche Altersvorsorge Weihnachtsgeld 30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] Homeoffice-Option Vergütung: 80.000-95.000 Euro brutto p. a. Für wen suchen wir Wir suchen für unseren Kunden, einem international agierenden Industrieunternehmen in Ingelheim, einen Patient Safety Physician/
Pharmacovigilance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Specialist/ Arzt Pharmaindustrie (m/w/d) in Vollzeit. Das bringen Sie mit Medizinischer Hintergrund: Sie sind approbierter Arzt (m/w/d) und verfügen über fundierte medizinische Kenntnisse Pharmakovigilanz-Kenntnisse: Sie haben ein tiefgehendes Verständnis der Pharmakovigilanz-Prozesse und regulatorischen Anforderungen in den wichtigsten Märkten (z. B. EU, USA) sowie der damit [. .. ]
▶ Zur Stellenanzeige
Job am 14.01.2026 bei Neuvoo gefunden
Cencora
[. .. ] and is specialized in all aspects of drugs and medical devices approval, of the market development and any action of effective product maintenance. We have an exciting [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] opportunity for a Pharmacovigilance Specialist to join us in Germany. You will be working on client projects, supporting their activities within Safety. Responsibilities: Set up and manage the local pharmacovigilance system Local Literature Search Local ICSR Management PV Intelligence Screening Local PSMF Maintenance Setting up local Organized Data Collection Local PVA Management Local adaptation and [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] safety-related documentation. Team Client Engagement: Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications: Medical Doctor [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise: Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge: Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation, and internal SOPs. Adaptability: Comfortable working in fast-paced environments with shifting priorities and deadlines. Communication Skills: Excellent verbal and written communication, able to convey complex ideas clearly to diverse audiences. Professional Credibility: Trusted medical professional with a strong foundation in both clinical and research settings. What We Offer [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] ensuring patient safety and regulatory compliance for assigned products in development and/or marketing. Providing medical analyses and input to meet international regulatory requirements and Companys objectives. Supporting [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the VP Pharmacovigilance in increasing the departments effectiveness and profile within Kyowa Kirin and the wider KHK Group. Supporting the Qualified Person for Pharmacovigilance in Europe by contributing to the constant improvement of the Kyowa Kirin Pharmacovigilance System. This position could be based in any of our UK or European based offices (France, [. .. ] the needs of the project team. Qualifications Position Requirements: MANDATORY: Medically qualified physician with post-registration clinical experience and a strong experience within pharmacovigilance or related area of clinical development; specialist training or clinical exposure in immunology and/or haemato oncology strongly preferred Knowledge of regulatory requirements pertaining to pharmacovigilance in the pre and post approval environments is preferred Fluent in English Excellent verbal, written, interpersonal, influencing and communication skills with emphasis on building consensus Ability to produce high quality, accurate [. .. ]
Job am 21.03.2026 bei Jobleads gefunden
• Berlin
[. .. ] restricted to, named patient programmes, accelerating patient recruitment for clinical trials, clinical protocol development, regulatory strategy and target product profile development. The MSL will be an important [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] member of a specialist launch team tasked with successfully launching the asset into Europe for our client. ESSENTIAL DUTIES AND RESPONSIBILITIES: Responsibilities KOL Stakeholder Engagement: Serve as the scientific representative for the organization throughout the brand lifecycle. Build and sustain mutually beneficial relationships with healthcare professionals who can be mobilized in support of the [. .. ] local laws and regulations as defined by the competent authorities Maintain up to date knowledge on any changes and share with internal organization where appropriate Ensure company is compliant with pharmacovigilance and adverse even reporting Ensure full adherence to EU, local (AIFA, MHRA, EMA) , and international regulations governing MSL activities and HCP engagement. Maintain up-to-date knowledge of EFPIA, ABPI (UK) , AIFA (Italy) , and other relevant codes of conduct. Document and report interactions and insights in compliance [. .. ]
Job am 28.02.2026 bei Jobleads gefunden
• Freiburg im Breisgau, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] Team management of a group of Global Safety Product Leads including leading, mentoring, and developing a team of Global Safety Product Leads, fostering a culture of compliance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and excellence. Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk profile Signal management: signal detection, signal validation, signal evaluation Risk management: preparation of risk management plans, supervision of risk minimization measures Preparation of periodic safety reports Supervision of interventional and non-interventional studies, as well as other data collection [. .. ] systematic documentation of reports on suspected cases of possible drug risks before and after receiving marketing authorization, from spontaneous reports, as part of post-marketing surveillance, from publications in the specialist literature and relevant databases. This includes the active and regular review of specialist literature and relevant databases with regard to published suspected cases of adverse drug reactions Fulfillment of all statutory notification and reporting obligations with regard to possible drug risks Evaluation of potential drug risks with simultaneous continuous updating [. .. ]
Job am 20.11.2025 bei Jobleads gefunden
• Köln, Nordrhein- Westfalen
[. .. ] (m/w/d) Cologne, North Rhine-Westphalia, Germany 1 week ago Cologne, North Rhine-Westphalia, Germany 5 days ago Cologne, North Rhine-Westphalia, Germany 2 weeks ago Regulatory Affairs-Labelling
Specialist (w/m/d) Langenfeld, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] North Rhine-Westphalia, Germany 2 weeks ago Global ICT Business Partner (Regulatory Affairs Pharmacovigilance) Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 70115425 [. .. ]
Job vor 4 Tagen bei Neuvoo gefunden
Wörwag Pharma
• Böblingen, Baden- Württemberg
Work-Life-Balance
[. .. ] collegial cooperation among our now 1, 200 employees worldwide. Become a part of our team in our headquarter in Böblingen (near Stuttgart) because we are looking for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you as a Specialist Medical Writing and Advice (m/w/d) These tasks await you Collaboration for preparation of parts of e CTD dossiers which are relevant for marketing authorisations in accordance with regulatory and internal specifications for European and global marketing authorisation Review and evaluation of the accuracy, consistency, and plausibility of externally produced clinical and non-clinical documents which are relevant for marketing authorisation Review and evaluation of information texts for medicinal products and food supplements Interface/ support of Regulatory Affairs and Global Pharmacovigilance in medical/ scientific issues Editing/ review of technical information and directions for use with regard to medico-scientifically relevant passages, e. g. , Originator adjustments, reviewing the Sm PC and PIL for Deficiency Letter answers in German for Biofactors portofolio Collaborating with the manager of the Generic portofolio, to complete Originator [. .. ]
Job vor 8 Tagen bei Neuvoo gefunden
Proclinical
• Leipzig, Saxony
Drive
specialist engagement and elevate access to rare disease treatments through strategic, insightsdriven account leadership. Proclinical is seeking a Key Account Manager to join a field-based team covering Leipzig [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and surrounding areas. In this role, you will focus on developing strong commercial relationships with healthcare professionals and decision-makers across hospitals [. .. ] boundaries. Collaborate with cross-functional teams, including Marketing, Medical Science Liaisons, and Market Access. Maintain accurate CRM records and report account plans and KPIs to senior management. Collect and report pharmacovigilance information as per internal SOPs. Represent the territory at national and international events and congresses. Key Skills and Requirements: A degree in a scientific or related field, or equivalent experience (e. g. , nursing, physiotherapy, clinical research) . Proven success in securing hospital formularies for complex products. Experience managing sales [. .. ]
Job am 27.03.2026 bei Neuvoo gefunden
EVERSANA
Medical Science Liaison
• Berlin
[. .. ] restricted to, named patient programmes, accelerating patient recruitment for clinical trials, clinical protocol development, regulatory strategy and target product profile development. The MSL will be an important [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] member of a specialist launch team tasked with successfully launching the asset into Europe for our client. ESSENTIAL DUTIES AND RESPONSIBILITIES: Responsibilities KOL Stakeholder Engagement: Serve as the scientific representative for the organization throughout the brand lifecycle. Build and sustain mutually beneficial relationships with healthcare professionals who can be mobilized in support of the [. .. ] and local laws and regulations as defined by the competent authorities Maintain upto date knowledge on any changes and share with internal organization where appropriate Ensure company is compliant with pharmacovigilance and adverse even reporting Ensure full adherence to EU, local (AIFA, MHRA, EMA) , and international regulations governing MSL activities and HCP engagement. Maintain up-to-date knowledge of EFPIA, ABPI (UK) , AIFA (Italy) , and other relevant codes of conduct. Document and report interactions and insights in compliance [. .. ]
Job am 26.03.2026 bei Neuvoo gefunden
Galderma
Customer Service Agent
• Düsseldorf, North Rhine- Westphalia
Betriebliche Altersvorsorge
[. .. ] das führende Unternehmen für Dermatologie weltweit zu werden. Mit uns haben Sie die ultimative Möglichkeit, neue und herausfordernde Arbeitserfahrungen zu sammeln und einen beispiellosen direkten Einfluss zu [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] erzielen. Customer Service Specialist (m/w/d) Standort: Düsseldorf (Hybrid) Als Customer Service Specialist (m/w/d) sind Sie die erste Ansprechperson für Apotheken, Ärztinnen und Ärzte sowie Patientinnen und Patienten. Sie betreuen eingehende Anfragen zu Produkten, Bestellungen und Services per Telefon und E-Mail und stellen eine serviceorientierte, regelkonforme Bearbeitung sicher. Sie dokumentieren [. .. ] Unterstützung im DACH-Umfeld Abwicklung von Reklamationen, Retouren und Gutschriften Durchführung von Outbound-Aktivitäten wie Follow-ups, Rückrufen sowie Informations- und Saleskampagnen Enge Zusammenarbeit mit internen Schnittstellen wie Medical Affairs, Pharmacovigilance, Quality, Finance und Vertrieb zur Klärung komplexer Anliegen Sicherstellung von Qualität, Compliance und korrekter Weiterleitung relevanter Informationen, beispielsweise zu Nebenwirkungsmeldungen Mitarbeit an Projekten zur Optimierung von Serviceprozessen, Customer Experience und Kundenbindung Ihr Profil Erfahrung im Customer Service, vorzugsweise in Pharma, Healthcare oder Life Sciences Abgeschlossenes Bachelor-Studium oder eine gleichwertige [. .. ]
Job am 06.02.2026 bei Neuvoo gefunden
Dr. Falk Pharma GmbH
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
• Freiburg im Breisgau, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] a team of Global Safety Product Leads, fostering a culture of compliance and excellence. Ensuring takeover of the following tasks and responsibilities of the Global Safety Product [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Leads group: Global pharmacovigilance product responsibility for the medicinal products Monitoring of the benefit-risk profile Signal management: signal detection, signal validation, signal evaluation Risk management: preparation of risk management plans, supervision of risk minimization measures Preparation of periodic safety reports Supervision of interventional and non-interventional studies, as well as other data collection [. .. ] systematic documentation of reports on suspected cases of possible drug risks before and after receiving marketing authorization, from spontaneous reports, as part of post-marketing surveillance, from publications in the specialist literature and relevant databases. This includes the active and regular review of specialist literature and relevant databases with regard to published suspected cases of adverse drug reactions Fulfillment of all statutory notification and reporting obligations with regard to possible drug risks Evaluation of potential drug risks with simultaneous continuous updating [. .. ]
Job am 27.11.2025 bei Neuvoo gefunden
Pro Pharma Group
Multilingual Medical Information Specialist-German Speaking
• Berlin
[. .. ] , Pro Pharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] compliance, pharmacovigilance, medical information, and R D technology, Pro Pharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. Were looking for a Multilingual Medical Information Specialist to join our Medical Information Department. You will be responsible for providing a high-quality Medical Information service via phone and email following full training on designated clients/ products. Were looking for candidates who can speak and write at C1 level in both German and English and we will offer [. .. ]
Job vor 11 Tagen bei Jooble gefunden
EVERSANA
Medical Science Liaison
• Berlin Berlin, DE
[. .. ] restricted to, named patient programmes, accelerating patient recruitment for clinical trials, clinical protocol development, regulatory strategy and target product profile development. The MSL will be an important [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] member of a specialist launch team tasked with successfully launching the asset into Europe for our client. ESSENTIAL DUTIES AND RESPONSIBILITIES: Responsibilities KOL Stakeholder Engagement: Serve as the scientific representative for the organization throughout the brand lifecycle. Build and sustain mutually beneficial relationships with healthcare professionals who can be mobilized in support of the [. .. ] local laws and regulations as defined by the competent authorities Maintain up to date knowledge on any changes and share with internal organization where appropriate Ensure company is compliant with pharmacovigilance and adverse even reporting Ensure full adherence to EU, local (AIFA, MHRA, EMA) , and international regulations governing MSL activities and HCP engagement. Maintain up-to-date knowledge of EFPIA, ABPI (UK) , AIFA (Italy) , and other relevant codes of conduct. Document and report interactions and insights in compliance [. .. ]
Job vor 11 Tagen bei Jooble gefunden
FERCHAU GmbH
Junior Specialist (m/w/d) Pharmacovigilance
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
Absolventen, Einsteiger, Trainees Abgeschlossene Ausbildung
Betriebliche Altersvorsorge Tarifvertrag
Ihr Aufgabengebiet Bearbeitung von Nebenwirkungsinformationen Informationszusammenstellung von Fallberichten und die fristgerechte Überprüfung von Nebenwirkungsmeldungen Datenverarbeitung in der Pharmakovigilanzdatenbank Mitarbeit bei der Überarbeitung von SOPs Unterstützung des/ der Stufenplanbeauftragten Das erwartet [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Sie bei uns Unbefristeter Arb [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Pharmacovigilance Specialist pro Jahr?
Als Pharmacovigilance Specialist verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmacovigilance Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 16 offene Stellenanzeigen für Pharmacovigilance Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmacovigilance Specialist Jobs?
Aktuell suchen 10 Unternehmen nach Bewerbern für Pharmacovigilance Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmacovigilance Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmacovigilance Specialist Stellenangebote:
- EVERSANA (2 Jobs)
- Proclinical (1 Job)
- Office Events Wiesbaden (1 Job)
- Galderma (1 Job)
- Dr. Falk Pharma GmbH (1 Job)
In welchen Bundesländern werden die meisten Pharmacovigilance Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Specialist Jobs werden derzeit in Berlin (4 Jobs), Nordrhein-Westfalen (3 Jobs) und Baden-Württemberg (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Specialist Jobs?
Pharmacovigilance Specialist Jobs gehören zum Berufsfeld Pharmazie.
