58 Jobs für Pharmacovigilance Manager
Stellenangebote Pharmacovigilance Manager Jobs
Job am 22.09.2026 bei Mindmatch.ai gefunden
headcount
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
headcount, a Swiss-based biotech, is seeking a Regional
Pharmacovigilance Manager to oversee PV and ICSR processes across regions. The role is remote with strong crossfunctional collaboration, vendor management, and regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] alignment. You will bring 510 years in pharmacovigilance, experience with safety databases, GVP, and fluent English, plus a scientific degree. The package includes a competitive salary, annual bonus, equity, and [. .. ]
Job am 22.09.2026 bei Mindmatch.ai gefunden
headcount
Regional Pharmacovigilance Manager
• AT- 2 Lavamünd
Regional
Pharmacovigilance Manager, Swiss-based (remote) Do you know how to keep regional pharmacovigilance running smoothly across systems, vendors and global teams? For a growing global biotech, we are looking for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a handson Regional Pharmacovigilance Manager to strengthen its Global Patient Safety organisation. The role Oversee regional PV and ICSR processes Manage external [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Führungs-/ Leitungspositionen
EVER Pharma invites a Global
Pharmacovigilance Manager to ensure compliant PV operations across international markets. You will coordinate PV activities, oversee PSMF sections and support inspections in a multinational environment. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The role requires a university degree in life sciences, strong knowledge of EU GVP and ICH guidance, and excellent English. Salary starts at 60, 977.70 plus [. .. ]
Job vor 7 Tagen bei StepStone gefunden
Esteve Pharmaceuticals GmbH
Product Manager Specialty Care (Mepact und Increlex) (m/w/d)
• Berlin
Betriebliche Altersvorsorge 30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] ihr Wohlbefinden. Wir sind stolz auf unser vielfältiges und inklusives Arbeitsumfeld, das dazu beiträgt, dass jeder Mitarbeiter sein volles Potenzial ausschöpfen kann. Wir suchen mit sofortiger Wirkung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] einen/ eine Product Manager Specialty Care (Mepact und Increlex) (m/w/d) Was Sie erwartet: Der Produktmanager für Mepact und Increlex ist verantwortlich für die Entwicklung und Umsetzung der kommerziellen Strategie für zwei spezialisierte Produkte im Bereich seltener Erkrankungen. Die Rolle umfasst die Analyse von Markt- und Patientenbedürfnissen, die Entwicklung von Markenstrategien sowie die [. .. ] effizienten Ressourceneinsatzes Aufbau und Pflege vertrauensvoller Beziehungen zu relevanten Experten, Behandlungszentren und Fachgesellschaften sowie Einbindung von Patientenperspektiven Enge Zusammenarbeit mit internen Schnittstellen wie Medical Affairs, Market Access, Sales, Regulatory Affairs, Pharmacovigilance und Supply Chain Unterstützung wissenschaftlicher Veranstaltungen, Kongresse und Fortbildungsinitiativen Leitung und Koordination cross-funktioner produktbezogener Projekte und Launch-Initiativen Steuerung externer Agenturen, Dienstleister und Partner unter Einhaltung regulatorischer und Compliance-Anforderungen Verantwortung für Umsatz-, Marktanteils- und Performance-Ziele der Produkte inkl. Forecasts Erstellung regelmäßiger Business Reviews und Unterstützung der [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
CSL
• AT- 9 Wien
Quality
Manager (m/f/x) - EU-based Location: Open to candidates based in countries where CSL has an affiliate presence, provided they are located within commuting distance of a CSL office and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] can attend the workplace in line with CSLs return-to-office policy. Employment: Full-time, Permanent You will be [. .. ] harmonization, and the implementation of global quality initiatives. This position offers the opportunity to influence quality practices across a complex international environment while collaborating with colleagues from Quality, Regulatory Affairs, Pharmacovigilance, Commercial Operations, Manufacturing, Compliance, and other business functions. The Role: Reporting to the Affiliate Quality Head, US Quality Systems, Standards Governance, you will: Establish and maintain processes for reporting Quality KPIs across global affiliates. Coordinate inspection readiness activities throughout the global affiliate network. Support quality management system compliance activities, ensuring [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Amgen
Senior Associate Global Safety (Local Safety Switzerland)
• AT- 2 Lavamünd
[. .. ] us. SENIOR ASSOCIATE GLOBAL SAFETY (LOCAL SAFETY SWITZERLAND) LIVE What you will do In this vital role as a Senior Associate Global Safety (Local Safety Switzerland) you [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] will support local pharmacovigilance activities in Switzerland and support provision of safety expertise to the local business. You will conduct core safety activities including data collection, processing, distribution and regulatory submission, based on appropriate training and assigned roles within the safety database and related systems. You will maintain compliance with Swiss legislation, Amgen policies and procedures, support the Safety Manager across the full range of local safety activities, and contribute safety expertise to local medical teams and cross-functional activities. The ability to identify, prioritize and elevate safety issues is important. The role works closely with colleagues in Germany and Austria and interacts regularly with Amgens international safety team worldwide. [. .. ]
Job am 01.10.2026 bei Mindmatch.ai gefunden
AOP Health
• AT- 9 Wien
[. .. ] and drive AOPs AI strategy, roadmap, governance framework, and enterprise-wide use-case portfolio, ensuring alignment with business priorities and measurable value creation. Partner with stakeholders across Medical, Regulatory, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Quality, Pharmacovigilance, Commercial, Manufacturing, Supply Chain, and Corporate Functions to identify, prioritize, and implement high-impact AI opportunities. Lead the responsible adoption of AI technologies by establishing governance standards, risk management practices, safe-use guidelines, and appropriate oversight for regulated and business-critical use cases. Coordinate cross-functional collaboration between business teams, [. .. ]
Job am 30.09.2026 bei Mindmatch.ai gefunden
Johnson Johnson
Key Account Manager Onkologie-Lunge (West Region)
• AT- 9 Wien
[. .. ] Ensures alignment of the all activities with J J Credo, applicable J J procedures and policies including but not limited to those related with Health Care Compliance, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical Research and Pharmacovigilance, GCPs, Regulatory Regulations and local Legislation Ensures safety reporting requirements (timely AE/ PQC reporting) as set out in company policies and SOPs (Standard Operating Procedures) are met and appropriately managed when planning projects Ensures HCC and legal requirements (Fair Market Value, Transferof Valuerules, Promotional Materialsrules) are fully understood, appropriately managed [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Berlin
Führungs-/ Leitungspositionen
[. .. ] therapies. 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. We are seeking an experienced and commercially driven Director of Business Development to lead strategic growth across [. .. ] based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office. Pro Pharma Group does not accept unsolicited resumes from recruiters/ third parties. Please, no phone calls or emails to anyone regarding this posting. [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Patient Safety Specialist (d/f/m)
• Holzkirchen, Bayern
Your Key Responsibilities Your responsibilities include, but are not limited to: Support the Senior
Manager Patient Safety in the coordination and execution of patient safety and
pharmacovigilance activities within [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Swiss affiliate. Act as Deputy Responsible Person for Pharmacovigilance Switzerland and provide support for local pharmacovigilance oversight activities in accordance with Swiss regulatory requirements. Promote understanding of the pharmacovigilance system across the Swiss affiliate and support adherence to local safety requirements, including implementation and tracking of Risk [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Holzkirchen, Bayern
Your responsibilities include, but are not limited to: Support the Senior
Manager Patient Safety in the coordination and execution of patient safety and
pharmacovigilance activities within the Swiss [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] affiliate. Act as Deputy Responsible Person for Pharmacovigilance Switzerland and provide support for local pharmacovigilance oversight activities in accordance with Swiss regulatory requirements. Promote understanding of the pharmacovigilance system across the Swiss affiliate and support adherence to local safety requirements, including implementation and tracking of Risk [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Director, Medical Affairs DACH
• München, Bayern
Führungs-/ Leitungspositionen
Corcept is seeking a Director, Medical Affairs DACH to lead all medical affairs activities across Germany, Austria, and Switzerland. Reporting to the DACH General
Manager with a dotted-line relationship [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to the Senior Director, Medical Affairs Europe, role will serve as the DACH senior medical authority for the affiliate, driving medical strategy, providing leadership to cross-functional partners, and ensuring alignment between European priorities and local execution while bringing DACH-specific insights to inform regional [. .. ] real-world evidence and other evidence-generation initiatives within DACH Monitor scientific and competitive developments and communicate actionable insights to regional and global stakeholders Serve as the medical counterpart to Pharmacovigilance for local safety-related activities and escalations Champion a culture of collaboration, accountability, and strategic execution, setting high standards for leadership effectiveness and cross-functional partnership Travel will be required for this role Preferred Skills, Qualifications and Technical Proficiencies: Strong understanding of German market access, AMNOG/ HTA processes and the [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
[. .. ] CRM Lead global patient safety strategy and shape the development of innovative medicines. As a Senior Patient Safety Physician, you will provide medical and strategic leadership across [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical development and pharmacovigilance activities, driving benefit-risk assessments and patient safety strategies for compounds in development and marketed products. Working within a global, cross-functional environment, you will play a key role in enabling informed development decisions and bringing meaningful therapeutic innovations to patients worldwide. This position can be filled in different countries. [. .. ] visibility of your profile-whether it should be confined to the recruiters managing the jobs you apply to, or be accessible to any company recruiter worldwide. Given that the hiring manager is not based in the country you are applying for and the interview process is performed in the hiring manager country, we kindly urge you to opt for Any company recruiter worldwide. This action will greatly assist us in processing your application in the most efficient manner, while ensuring compliance [. .. ]
Job am 09.09.2026 bei Jobleads gefunden
Legal Counsel, Regulatory Commercial International
• München, Bayern
Overview The Senior
Manager, Law and Compliance, Germany is based in Munich, Germany, and is a key member of the Incyte German team, and Incytes International Law and Compliance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team. The role reports to the Senior Director, Law and Compliance, DACH, located in Munich, Germany. The role will primarily provide legal support on ex-[. .. ] and national pharmaceutical law regulations; changes in European and national pharmaceutical law and industry standards, assessing their impact on Incyte; issues of labelling, packaging, patient information leaflets or similar documentation; pharmacovigilance, quality assurance, any product supply and recalls or issues potentially impacting patient safety; loss of exclusivity and protection of clinical data; training needs and risk mitigation within the organization and developing and arranging and/or presenting training sessions on relevant laws and legal, business or operational issues; and decisions, legislation, [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
• München, Bayern
[. .. ] future for patients, their families, and society. Purpose of the function This role supports the CSPV DSE SOP and Training Team Lead in the governance, maintenance and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] continuous improvement of Pharmacovigilance (PV) training activities and procedural documents within DSE and, where applicable, at global level. The position helps ensure that PV training processes and procedures are established and implemented in line with regulatory requirements, global standards and DSE expectations, while contributing to inspection readiness, compliance and continuous improvement. Roles and Responsibilities [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
Clinical Study Manager (m/w/d)
• München, Bayern
Homeoffice möglich Abgeschlossenes Studium
Flexible Arbeitszeiten
[. .. ] Vollzeit Über uns Für ein wachstumsstarkes Biotechnologieunternehmen mit Fokus auf die Entwicklung innovativer Therapien zur Verbesserung der Patientenversorgung suchen wir zur Verstärkung des Clinical Operations Teams einen [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] engagierten Clinical Trial Manager/ Clinical Study Manager (m/w/d) , der die Durchführung unserer klinischen Studien aktiv unterstützt und verantwortet. Ihre Aufgaben Eigenverantwortliche Planung, Durchführung und Überwachung nationaler und internationaler klinischer Studien der Phasen I-III. Steuerung und Koordination von CROs, Studienzentren, externen Dienstleistern und weiteren Studienpartnern. Sicherstellung der Durchführung von Studien gemäß [. .. ] der Auswahl, Initiierung und Betreuung von Prüfzentren. Management studienrelevanter Dokumentation, einschließlich Trial Master File (TMF) und essenzieller Studiendokumente. Enge Zusammenarbeit mit internen Funktionen wie Clinical Development, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Data Management und Biostatistics. Vorbereitung und Begleitung von Audits und Inspektionen. Analyse studienbezogener Kennzahlen sowie Erstellung von Statusberichten für das Management. Unterstützung bei der Entwicklung und Optimierung klinischer Prozesse und Standards. Erfolgreich abgeschlossenes Studium der Naturwissenschaften, Medizin, Pharmazie, Biotechnologie oder eines vergleichbaren Fachgebiets. Mindestens 2-3 Jahre Berufserfahrung im Bereich [. .. ]
Job gestern bei Jobleads gefunden
• Neuenburg
We are supporting a pharmaceutical organisation in Switzerland in the appointment of an experienced Regulatory Affairs
Manager to oversee regulatory submissions, marketing authorisations and lifecycle management for medicinal products [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] within the Swiss market. This is a hands-on position suited to a highly autonomous, pragmatic and commercially aware regulatory professional with extensive knowledge of Swissmedic requirements and Swiss pharmaceutical regulations. The successful candidate will take ownership of [. .. ] ensure compliance with Swiss pharmaceutical advertising requirements. Provide regulatory guidance to Medical, Commercial and Marketing teams. Support regulatory activities associated with product launches and commercialisation in Switzerland. Collaborate with Quality, Pharmacovigilance, Medical, Commercial, external manufacturers, suppliers and strategic partners. Maintain regulatory information systems, submission trackers and relevant regulatory documentation. Candidate Requirements Masters degree in Life Sciences, Pharmacy or a related scientific discipline. Minimum 8 years of experience in pharmaceutical Regulatory Affairs, with substantial hands-on experience in the Swiss market. Proven [. .. ]
Job gestern bei Jobleads gefunden
Clinical Research Lead-single-client-Germany
• München, Bayern
[. .. ] Monitors) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. Employs strategic thinking and problem-solving skills to propose and implement risk mitigations. Participates and presents in key meetings such as Kick Off Meeting. Serves as an escalation [. .. ] of other functions roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP and country regulations. This may include data management, study start up, patient recruitment, medical monitoring, pharmacovigilance and Quality Assurance (QA) . Supports Inspection Readiness for clinical trial management scope. Oversees CRAs and Central Monitors assigned to the study and routinely assesses study-specific process and training compliance, CMP compliance, and identifies emerging risks. May develop and support execution of corrective action plans at site and study [. .. ]
Job gestern bei Jobleads gefunden
• Frankfurt, Hesse
Work-Life-Balance
[. .. ] an impact and a team that cares about the people behind the work as much as the work itself, we would love to hear from you. Job [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Description The Site Manager (SM) is engaged in facilitating the conduct of clinical studies. Specific focus is put on patient related site support, with the aim to maximise the utilisation of site staff designated to a given study (e. g. study site coordinator, study nurse, sub-investigator) through provision of site training and oversight [. .. ] you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. Youll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting. We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here. Quality: we hold ourselves to the standard patients deserve. Integrity and trust: we do [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
RWE Delivery Manager-French/ Germany
Beratungs-/ Consultingtätigkeiten
[. .. ] pharmaceutical partners. Work with Medical, Clinical Operations, Data, Legal and Quality teams, and turn delivery experience into reusable methods. Your Team Your future colleagues: youll work closely [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with Mehdi, Project Manager RWE, on study delivery and shared project-management practices, and with Maxime and Eugnie, Global Pharma Partners, to connect pharmaceutical partners needs with practical study execution. Your manager: youll report to Adil, RWE Lead, who leads Resiliences Real-World Evidence activities. Adil gives you room to own your projects, with [. .. ] Navigate the German research environment: ethics committees, GDPR/ DSGVO, Länder-level data protection requirements and hospital contracting. Oversee a CRO and its deliverables, with a clear understanding of sponsor responsibilities, pharmacovigilance and monitoring plans. Track a study budget and make variances, risks and necessary trade-offs visible. Assess clinical data quality and discuss electronic health record structuring and AI-assisted extraction. Work fluently in German and use professional English in writing and speaking. You are the right person if you have [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
RWE Delivery Manager-French/ Germany
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] pharmaceutical partners. Work with Medical, Clinical Operations, Data, Legal and Quality teams, and turn delivery experience into reusable methods. Your Team Your future colleagues: youll work closely [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with Mehdi, Project Manager RWE, on study delivery and shared project-management practices, and with Maxime and Eugnie, Global Pharma Partners, to connect pharmaceutical partners needs with practical study execution. Your manager: youll report to Adil, RWE Lead, who leads Resiliences Real-World Evidence activities. Adil gives you room to own your projects, with [. .. ] Navigate the German research environment: ethics committees, GDPR/ DSGVO, Länder-level data protection requirements and hospital contracting. Oversee a CRO and its deliverables, with a clear understanding of sponsor responsibilities, pharmacovigilance and monitoring plans. Track a study budget and make variances, risks and necessary trade-offs visible. Assess clinical data quality and discuss electronic health record structuring and AI-assisted extraction. Work fluently in German and use professional English in writing and speaking. You are the right person if you have [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Quality Manager (m/f/x) - EU-based
• München, Bayern
Quality
Manager (m/f/x) - EU-based Location: Open to candidates based in countries where CSL has an affiliate presence, provided they are located within commuting distance of a CSL office [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and can attend the workplace in line with CSLs return-to-office policy. Employment: Full-time, Permanent You will be [. .. ] harmonization, and the implementation of global quality initiatives. This position offers the opportunity to influence quality practices across a complex international environment while collaborating with colleagues from Quality, Regulatory Affairs, Pharmacovigilance, Commercial Operations, Manufacturing, Compliance, and other business functions. The Role: Reporting to the Affiliate Quality Head, US Quality Systems, Standards Governance, you will: Establish and maintain processes for reporting Quality KPIs across global affiliates. Coordinate inspection readiness activities throughout the global affiliate network. Support quality management system compliance activities, ensuring [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Quality Manager (m/f/x) - EU-based
• Wien
Quality
Manager (m/f/x) - EU-based Location: Open to candidates based in countries where CSL has an affiliate presence, provided they are located within commuting distance of a CSL office [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and can attend the workplace in line with CSLs return-to-office policy. Employment: Full-time, Permanent You will be [. .. ] harmonization, and the implementation of global quality initiatives. This position offers the opportunity to influence quality practices across a complex international environment while collaborating with colleagues from Quality, Regulatory Affairs, Pharmacovigilance, Commercial Operations, Manufacturing, Compliance, and other business functions. The Role: Reporting to the Affiliate Quality Head, US Quality Systems, Standards Governance, you will: Establish and maintain processes for reporting Quality KPIs across global affiliates. Coordinate inspection readiness activities throughout the global affiliate network. Support quality management system compliance activities, ensuring [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Associate Director, Commercial Operations
• Zug
Führungs-/ Leitungspositionen
[. .. ] onsite presence in Zug, offering the opportunity to be deeply integrated into Mirums company culture. Remote working is permitted in accordance with Mirum policy and as agreed [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the reporting manager. JOB FUNCTIONS/ RESPONSIBILITIES Forecasting Business Planning Lead the development, maintenance, and continuous improvement of commercial forecasting models across brands and countries. Partner with Country General Managers, Brand Leads, Finance, and Commercial Leadership and facilitate the creation update of country level mid long-range forecasts Ensure forecasts are transparent, assumption-driven, [. .. ] and commercial signals) . Translate findings and competitive developments into actionable commercial implications for brand strategy, forecasting, launch planning, and decision-making. Ensure compliance with internal legal, procurement, compliance, and pharmacovigilance requirements. Manage Sales Incentive Plans for country sales teams, including plan design, target setting, performance tracking, calculation, reconciliation, communication, exception management and coordination of payouts in partnership with key stakeholders. Own the commercial administration of Veeva CRM for Mirum International, including users, territories, targeting lists and relevant field configurations; provide [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Manager Medical Safety
• Neuenburg
[. .. ] join us, youll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions. Were [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] looking for a Manager Medical Safety located in Neuchatel to provide robust safety expertise for assigned products through lifecycle management. Impact Youll Own Be responsible for the product safety surveillance program Oversee adverse events collection, evaluation, processing, assessment, reporting during and after clinical studies and post marketing safety surveillance. What Youll Do Ensure review/medical assessment of reported adverse events and serious adverse events. Apply standard pharmacovigilance procedures and guarantee compliance with requirements for adverse events assessment and regulatory reporting. Support and review study protocol writing including all clinical study related documents; review of Safety Update Reports (SURs) . Provide clinical information and safety reports as required by regulatory agencies/ ethics committees (from clinical studies and consumer [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Pharmacovigilance Manager pro Jahr?
Als Pharmacovigilance Manager verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmacovigilance Manager Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 58 offene Stellenanzeigen für Pharmacovigilance Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmacovigilance Manager Jobs?
Aktuell suchen 7 Unternehmen nach Bewerbern für Pharmacovigilance Manager Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmacovigilance Manager Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmacovigilance Manager Stellenangebote:
- headcount (2 Jobs)
- Esteve Pharmaceuticals GmbH (1 Job)
- CSL (1 Job)
- Amgen (1 Job)
- AOP Health (1 Job)
- Johnson Johnson (1 Job)
In welchen Bundesländern werden die meisten Pharmacovigilance Manager Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Manager Jobs werden derzeit in Bayern (18 Jobs), Niedersachsen (5 Jobs) und Berlin (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Manager Jobs?
Pharmacovigilance Manager Jobs gehören zum Berufsfeld Pharmazie.
