14 Jobs für Pharmacovigilance Consultant
Stellenangebote Pharmacovigilance Consultant Jobs
Job vor 3 Tagen 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 [. .. ] and reporting obligations with regard to possible drug risks Evaluation of potential drug risks with simultaneous continuous updating of the benefit-risk assessment, if necessary with the involvement of a consultant human physician Coordination of risk prevention measures as part of the action plan Updating the action plan and its monitoring and compliance Informing the competent authority (ies) about quality defects that could lead to a recall or an unusual restriction of distribution Informing the competent authority (ies) of any suspicion [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Veeva Systems
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] of choice for 85 of the top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy Operations as well as Quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Safety (eg. Pharmacovigilance) . As a Senior Consultant, you will manage complex and novel consulting projects for Veeva customers in the research and development (R D) space managing teams and planning, organizing, and tracking all aspects of delivery. You will analyze interesting problems, build insightful solutions, and develop close working relationships with stakeholders to deliver realizable value, at [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Dr. Falk Pharma GmbH
• Regierungsbezirk Freiburg
[. .. ] 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 Supervision of interventional and non-interventional studies, as well as other data collection activities including preparation and review [. .. ] system to fulfill all relevant pharmacovigilance obligations of Dr. Evaluation of potential drug risks with simultaneous continuous updating of the benefit-risk assessment, if necessary with the involvement of a consultant human physician Updating the action plan and its monitoring and compliance Coordination of a step-by-step plan procedure with the competent federal authority, the supervisory authorities and, if applicable, competent associations such as BPI (German Pharmaceutical Industry Association) , BAH (German Association of Pharmaceutical Manufacturers) and Vf A (Association of [. .. ]
Job vor 3 Tagen 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 [. .. ] and reporting obligations with regard to possible drug risks Evaluation of potential drug risks with simultaneous continuous updating of the benefit-risk assessment, if necessary with the involvement of a consultant human physician Coordination of risk prevention measures as part of the action plan Updating the action plan and its monitoring and compliance Informing the competent authority (ies) about quality defects that could lead to a recall or an unusual restriction of distribution Informing the competent authority (ies) of any suspicion [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Dr. Falk Pharma GmbH
• Regierungsbezirk Freiburg
[. .. ] 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 Supervision of interventional and non-interventional studies, as well as other data collection activities including preparation and review [. .. ] system to fulfill all relevant pharmacovigilance obligations of Dr. Evaluation of potential drug risks with simultaneous continuous updating of the benefit-risk assessment, if necessary with the involvement of a consultant human physician Updating the action plan and its monitoring and compliance Coordination of a step-by-step plan procedure with the competent federal authority, the supervisory authorities and, if applicable, competent associations such as BPI (German Pharmaceutical Industry Association) , BAH (German Association of Pharmaceutical Manufacturers) and Vf A (Association of [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Dr. Falk Pharma GmbH
• Regierungsbezirk Freiburg
[. .. ] 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 Supervision of interventional and non-interventional studies, as well as other data collection activities including preparation and review [. .. ] system to fulfill all relevant pharmacovigilance obligations of Dr. Evaluation of potential drug risks with simultaneous continuous updating of the benefit-risk assessment, if necessary with the involvement of a consultant human physician Updating the action plan and its monitoring and compliance Coordination of a step-by-step plan procedure with the competent federal authority, the supervisory authorities and, if applicable, competent associations such as BPI (German Pharmaceutical Industry Association) , BAH (German Association of Pharmaceutical Manufacturers) and Vf A (Association of [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Veeva Systems
Senior Business Consultant-R D (Remote)
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] of choice for 85 of the top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy Operations as well as Quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Safety (eg. Pharmacovigilance) . As a Senior Consultant, you will manage complex and novel consulting projects for Veeva customers in the research and development (R D) space managing teams and planning, organizing, and tracking all aspects of delivery. You will analyze interesting problems, build insightful solutions, and develop close working relationships with stakeholders to deliver realizable value, at [. .. ]
Job am 11.01.2026 bei Jobleads gefunden
• Genf
[. .. ] de la prescription constitue un axe essentiel du service, en particulier chez la patientle vulnrable (enfants, personnes ges, psychiatriques) . Le service est le centre rgional de [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] rfrence pour la pharmacovigilance. Il assure par ailleurs une prise en charge multidisciplinaire reconnue dans le domaine de la douleur. Dans lensemble de ces domaines, le service dispense un enseignement et une recherche dexcellence. Description Du Poste Votre mission alterne entre la supervision des diffrentes consultations de la pharmacologie et toxicologie cliniques, savoir la [. .. ] risque et de personnaliser les traitements (polymdication, interactions mdicamenteuses, adaptation la fonction rnale ou hpatique, observance) . Vous participez galement aux diffrentes activits du service. Vous exercez une activit de consultant ou consultante auprs des personnes hospitalises ainsi quune activit ambulatoire en pharmacologie et toxicologie cliniques. Qualifications Vous tes titulaire du diplme de mdecin fdral suisse ou disposez dune formation juge quivalente par la Commission des professions mdicales (MEBEKO) . Par ailleurs, vous disposez dun titre de spcialiste en Pharmacologie et [. .. ]
Job am 20.11.2025 bei Jobleads gefunden
• Köln, Nordrhein- Westfalen
[. .. ] North Rhine-Westphalia, Germany 2 weeks ago Manager (w/m/d) Regulatory Affairs Biocides Cologne, North Rhine-Westphalia, Germany 1 week ago Regulatory Change Manager, Compliance (m/f/d) Senior
Consultant Regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Affairs/ Life Sciences (m/w/d) Manager (m/w/d) Product Information Regulatory Affairs Neuss, North Rhine-Westphalia, Germany 6 hours ago Neuss, North Rhine-Westphalia, Germany 2 weeks ago Senior Manager Regulatory Reporting/ Bankenumfeld (m/w/d) Consultant Quality Assurance and Regulatory Affairs (m/w/d) Bonn, North [. .. ] ago Cologne, North Rhine-Westphalia, Germany 2 weeks ago Regulatory Affairs-Labelling Specialist (w/m/d) 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 05.09.2025 bei Jobleads gefunden
• Berlin
Beratungs-/ Consultingtätigkeiten
Overview Join to apply for the Business
Consultant-R D (Remote) role at Veeva Systems. Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] bring therapies to patients faster. As one of the fastest-growing Saa S companies in history, we surpassed 2B in revenue in our last fiscal year with extensive [. .. ] for 85 of the top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy Operations as well as Quality and Safety (e. g. , Pharmacovigilance) . As a Consultant, you will manage workstreams on consulting projects for Veeva customers in R D planning, organizing, and tracking all aspects of delivery. You will analyze problems, build insightful solutions, and develop close working relationships with customer stakeholders (through face-to-face discussions, workshops, email, etc. ) to [. .. ]
Job am 20.08.2025 bei Jobleads gefunden
Deputy Responsible Person Wholesale/ QM Manager GDP
• München, Bayern
[. .. ] risk, deviation and CAPA management Document management Carrying out internal and external audits Creation and management of quality-related documents and contracts Communicating internally with colleagues in the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relevant Sales, Pharmacovigilance and Medical Affairs departments and externally with employees of contracted service providers regarding GMP/ GDP-related issues and problems Personal skills and professional experience University/ FH/ Masters degree in natural sciences or pharmacy or equivalent qualification Knowledge of the relevant laws, regulations and guidelines (AMG, AM-Handels V) Experience and knowledge [. .. ] for Quality Assurance Manager roles. Quality Assurance Manager Quality Operations Shopfloor (f/m/d) Quality Assurance Manager-Quality Operations Shopfloor (f/m/d) Quality Assurance Manager (m/w/d) Airbus Consultant Supply Chain and Supplier Quality Assurance Manager (m/w/d) Education and Quality Assurance Manager (m/w/d) Sr Process Improvement Manager FTC-1 year, Fleet Physical Supply Chain Working Student-Enterprise Data Operations (f/m/D) Were unlocking community knowledge in a new way. Experts add insights directly into [. .. ]
Job vor 2 Tagen bei Neuvoo.com gefunden
Dr. Falk Pharma GmbH
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
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 [. .. ] and reporting obligations with regard to possible drug risks Evaluation of potential drug risks with simultaneous continuous updating of the benefit-risk assessment, if necessary with the involvement of a consultant human physician Coordination of risk prevention measures as part of the action plan Updating the action plan and its monitoring and compliance Informing the competent authority (ies) about quality defects that could lead to a recall or an unusual restriction of distribution Informing the competent authority (ies) of any suspicion [. .. ]
Job vor 3 Tagen 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 [. .. ] and reporting obligations with regard to possible drug risks Evaluation of potential drug risks with simultaneous continuous updating of the benefit-risk assessment, if necessary with the involvement of a consultant human physician Coordination of risk prevention measures as part of the action plan Updating the action plan and its monitoring and compliance Informing the competent authority (ies) about quality defects that could lead to a recall or an unusual restriction of distribution Informing the competent authority (ies) of any suspicion [. .. ]
Job am 14.01.2026 bei Neuvoo gefunden
Cencora
Global Commercialisation Launch Lead
Führungs-/ Leitungspositionen
[. .. ] thinking leader in the industry, focused on growing this business segment within Cencoras International Business Group (IBG) and Global Pharma Services (GPS) covering various commercialization offerings including [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory, market access, Pharmacovigilance, distribution, logistics and Patient services. Key Responsibilities Lead the Customer experience model for small to mid size customers and ensure the customer is receiving a seamless centralized launch experience while also managing internal Cencora stakeholders Own and refine the Product Launch Process developing area expertise within Cencora to create a [. .. ] complex cross-functional projects within the pharmaceutical or healthcare industry Demonstrated success in launching new products into the US or Europe/ global from a pharma perspective and with a manufacturer/ consultant/ supplier profile Broad knowledge of brand/product launch across all global markets In-depth understanding of the US or European pharmaceutical landscape, including market access, quality, regulatory affairs, pharmacovigilance, compliance, distribution, 3PL, patient services, and sales marketing Excellent interpersonal and communication skills, with the ability to collaborate effectively with individuals [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Pharmacovigilance Consultant pro Jahr?
Als Pharmacovigilance Consultant verdient man zwischen EUR 50.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmacovigilance Consultant Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 14 offene Stellenanzeigen für Pharmacovigilance Consultant Jobs.
In welchen Bundesländern werden die meisten Pharmacovigilance Consultant Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Consultant Jobs werden derzeit in Niedersachsen (2 Jobs), Nordrhein-Westfalen (1 Jobs) und Baden-Württemberg (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Consultant Jobs?
Pharmacovigilance Consultant Jobs gehören zum Berufsfeld Pharmazie.
