14 Jobs für Pharmacovigilance Specialist
Stellenangebote Pharmacovigilance Specialist Jobs
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 06.02.2026 bei StepStone gefunden
Dr. Falk Pharma GmbH
• Freiburg
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] 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 vor 12 Tagen bei Mindmatch.ai gefunden
Sandoz International GmbH
• AT- 7 Kundl
Teilzeit Homeoffice möglich
Senior Regulatory
Specialist (d/f/m) Part-Time 80 Sandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. By creating [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a new and ambitious path, it will provide a unique opportunity for us all, both professionally and personally. Are you [. .. ] approval of proposed labeling updates. Continuously monitor and contribute to the enhancement of labeling processes, quality standards, and digital systems/ tools. Collaborate effectively with cross-functional stakeholders including Regulatory Affairs, Pharmacovigilance, Medical Affairs, and Commercial teams to ensure labeling consistency and compliance. Represent the Global Labeling function in cross-functional project teams and regulatory forums, contributing subject matter expertise and strategic insights. What youll bring to the role: Scientific academic degree (MSc, Ph D or comparable degree) , preferably in natural sciences [. .. ]
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 4 Tagen bei Jobleads gefunden
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
• 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 vor 12 Tagen bei Jobleads gefunden
Senior Regulatory Specialist (d/f/m) Part-Time 80
• Kundl, Tirol
Homeoffice möglich
Senior Regulatory
Specialist (d/f/m) Part-Time 80 Sandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. By creating [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a new and ambitious path, it will provide a unique opportunity for us all, both professionally and personally. Are you [. .. ] approval of proposed labeling updates. Continuously monitor and contribute to the enhancement of labeling processes, quality standards, and digital systems/ tools. Collaborate effectively with cross-functional stakeholders including Regulatory Affairs, Pharmacovigilance, Medical Affairs, and Commercial teams to ensure labeling consistency and compliance. Represent the Global Labeling function in cross-functional project teams and regulatory forums, contributing subject matter expertise and strategic insights. What youll bring to the role: Scientific academic degree (MSc, Ph D or comparable degree) , preferably in natural sciences [. .. ]
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) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Langenfeld, 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 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
• 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 am 21.11.2025 bei Neuvoo gefunden
CHEPLAPHARM Arzneimittel GmbH
• Berlin
Senior
Specialist Supply Projects (m/f/d) Berlin Greifswald Vollzeit We are a global and growing speciality pharmaceutical company with an exceptional, sustainable business model. Our mission : to be THE [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] platform for established and trusted branded products in various therapeutic areas and indications and to ensure their availability in the highest [. .. ] engineering, or a comparable field Required professional experience: 5 years, ideally in the area of supply chain or project management Alternatively, you have experience in regulatory affairs, quality assurance, or pharmacovigilance You already have some experience in coordinating cross functional teams and complex projects You are characterized by analytical thinking and a structured and results-oriented approach to work You communicate and negotiate confidently in German and English and have a good working knowledge of MS Office; knowledge of SAP is [. .. ]
Job am 18.11.2025 bei Neuvoo gefunden
CHEPLAPHARM Arzneimittel GmbH
Senior Specialist Supply Projects (m/f/d)
• Greifswald, Mecklenburg- Vorpommern
Senior
Specialist Supply Projects (m/f/d) Berlin Greifswald Vollzeit We are a global and growing speciality pharmaceutical company with an exceptional, sustainable business model. Our mission : to be THE [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] platform for established and trusted branded products in various therapeutic areas and indications and to ensure their availability in the highest [. .. ] engineering, or a comparable field Required professional experience: 5 years, ideally in the area of supply chain or project management Alternatively, you have experience in regulatory affairs, quality assurance, or pharmacovigilance You already have some experience in coordinating cross functional teams and complex projects You are characterized by analytical thinking and a structured and results-oriented approach to work You communicate and negotiate confidently in German and English and have a good working knowledge of MS Office; knowledge of SAP is [. .. ]
Job am 20.10.2025 bei Neuvoo gefunden
Pro Pharma Group
Multilingual Medical Information Specialist-Norwegian Speaking
• germany,
[. .. ] , 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 are able to speak and write in Norwegian and English at C1 level and we will [. .. ]
Job am 13.02.2026 bei Jooble gefunden
FERCHAU GmbH
Junior Specialist (m/w/d) Pharmacovigilance
• Frankfurt am Main
Absolventen, Einsteiger, Trainees Abgeschlossene Ausbildung
Betriebliche Altersvorsorge Tarifvertrag
Menschen und Technologien verbinden. Den Perfect Match für unsere Kunden gestalten. Immer die richtigen Expert:innen für die jeweilige Herausforderung finden-das ist unser Anspruch bei FERCHAU und dafür suchen wir Sie: [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] als Mitarbeiter:in für einen unserer Kunden. Wir realisieren spannende Projekte für namhafte Kunden in den Bereichen Pharma und Li [. .. ]
Job am 06.02.2026 bei Jooble gefunden
Dr. Falk Pharma GmbH
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
• Regierungsbezirk Freiburg
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 [. .. ]
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 14 offene Stellenanzeigen für Pharmacovigilance Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmacovigilance Specialist Jobs?
Aktuell suchen 7 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:
- Dr. Falk Pharma GmbH (3 Jobs)
- Pro Pharma Group (2 Jobs)
- CHEPLAPHARM Arzneimittel GmbH (2 Jobs)
- Sandoz International GmbH (1 Job)
- Cencora (1 Job)
- FERCHAU GmbH (1 Job)
In welchen Bundesländern werden die meisten Pharmacovigilance Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Specialist Jobs werden derzeit in Niedersachsen (3 Jobs), Baden-Württemberg (2 Jobs) und Berlin (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Specialist Jobs?
Pharmacovigilance Specialist Jobs gehören zum Berufsfeld Pharmazie.
