29 Jobs für Pharmacovigilance Manager
Stellenangebote Pharmacovigilance Manager Jobs
Job gestern 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 gestern 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 11 Tagen bei JobMESH gefunden
Dr. Theiss Naturwaren GmbH
Medical Affairs Manager (m/w/d) - Scientific Information Regulatory Affairs.
• Saarland Homburg
Abgeschlossenes Studium
30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] werden unsere innovativen Apothekenprodukte mit renommierten Auszeichnungen wie Beste Neueinführung oder Top Marke geehrt. Für die medizinisch-wissenschaftliche Betreuung unseres Arzneimittelportfolios suchen wir zum nächstmöglichen Zeitpunkt eine/n Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Affairs Manager (m/w/d) Scientific Information Regulatory Affairs. In dieser Funktion sind Sie ferner als Informationsbeauftragter gemäß 74a Arzneimittelgesetz (Deutschland) sowie 56 Arzneimittelgesetz (Österreich) tätig und stellen die Einhaltung der relevanten gesetzlichen und regulatorischen Anforderungen sicher. Sie arbeiten eng mit Regulatory Affairs, Pharmacovigilance, Marketing, Vertrieb sowie externen Partnern und Behörden zusammen und begleiten wissenschaftliche Fragestellungen über den gesamten Produktlebenszyklus. Ihre Aufgaben Wahrnehmung der Funktion des Informationsbeauftragten gemäß deutschem und österreichischem Arzneimittelgesetz Ansprechpartner für Behörden, Fachkreise, Außendienst und Verbraucher bei medizinisch-wissenschaftlichen Fragestellungen Erstellung, Bewertung und Pflege von Fachinformationen, Gebrauchsinformationen, Produktinformationen und Pflichttexten Erstellung [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Novartis
• AT- 2 Schweiz
Job Description Summary The Development Quality Assurance
Manager is responsible for assuring quality over-sight for activities undertaken in all Novartis entities in a country to assure compliance with relevant Good [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical Practice (GCP) and Good Pharmacovigilance Practice (GPv P) regulations and guidelines to assure the execution of high quality research and activities within a country (ies) . Activities in scope include but may not be limited to assuring adequate systems are in place for the protection of patient safety, rights and well-being, data integrity, and quality [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Gouya Insights
Clinical Project Manager
• AT- 9 Wien
Looking for an opportunity to put your clinical project management skills to the test? We are seeking an experienced Clinical Project
Manager to join our team at Gouya Insights Gmb [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] H Co KG, a clinical development consulting and clinical research services company supporting innovative biotech, pharmaceutical, and medical device companies. As Clinical Project Manager, you will take operational ownership of early-phase clinical studies and development projects, working at the interface between our [. .. ] and crossfunctional experts. Track criticalpath activities and proactively identify, elevate, and resolve operational risks, issues, and dependencies. Coordinate crossfunctional activities with Medical Experts and Medical Writers, Clinical Data Management, Biostatistics, Pharmacovigilance, and Quality. Maintain effective project governance, including project, risk, and action trackers, status reporting, and project meetings. Support clinical trial budget management, forecasting, accruals, and change control. Lead the selection, coordination, and oversight of CROs and specialist clinical trial vendors and support their contracting and qualification. Review scopes of work, [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
Amgen Inc. (IR)
• 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 vor 14 Tagen 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 team. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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
[. .. ] protecting the confidentiality of each subject/ patient. Assess factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records. [. .. ] off visits for junior CRA staff, as assigned. May be mentored and assigned clinical operations lead tasks under supervision of an experienced Clinical Operations Lead (COL) , or operational line manager. Qualifications Bachelors degree or RN in a related field or equivalent combination of education, training and experience Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Previous monitoring experience in Germany Must demonstrate good computer skills and be able to embrace new technologies Fluency in German and [. .. ]
Job gestern bei Jobleads gefunden
Responsable assurance qualit
• Neuenburg
[. .. ] Commencement: October 2026 or at a mutually agreed date Languages Required: English (C1) and French (C1) or German (C1) . About the Role We are seeking an [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experienced Quality Affairs Manager to lead quality activities related to the distribution and commercialisation of medicinal products in Switzerland. The candidate will take responsibility for the maintenance and continuous improvement of the Quality Management System (QMS) , ensure compliance with Good Distribution Practice (GDP) requirements and oversee quality activities related to the storage, distribution [. .. ] and distribution activities. Monitor developments in Swiss GDP requirements and applicable Swissmedic technical interpretations and assess their impact on the companys activities and Quality Management System. Collaborate with Regulatory Affairs, Pharmacovigilance, Commercial and other internal functions on quality matters related to medicinal products. Act as a key point of contact for pharmaceutical quality matters with suppliers, logistics providers, partners and competent authorities. Requirements Masters degree in Life Sciences, Pharmacy or another relevant scientific discipline. Minimum of 8 years of experience in [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Development Quality Assurance Manager/ Expert
• Schweiz, Kärnten
Job Description Summary The Development Quality Assurance
Manager is responsible for assuring quality over-sight for activities undertaken in all Novartis entities in a country to assure compliance with relevant [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GPv P) regulations and guidelines to assure the execution of high quality research and activities within a country (ies) . Activities in scope include but may not be limited to assuring adequate systems are in place for the protection of patient safety, rights and well-being, data integrity, and quality [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Regional Account Manager, Neurofibromatosis Region Süd-West (Freiburg, Stuttgart, Mannheim, He. . .
• München, Bayern
This Is What You Will Do The Regional Key Account
Manager, Koselugo will develop commercial relationships and value-adding activities in collaboration with key decision makers to maximize access to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] products within key accounts/ hospitals identified in the region. The position requires a strong business acumen, an entrepreneurial mindset, and the ability to work collaboratively within a complex hospital account environment. [. .. ] of Alexion with relevant customer groups Timely and complete reporting and presentation of account plans including KPIs to senior positions and accurate maintenance of the CRM database Collect and report pharmacovigilance information according to internal SOPs Represent their territories in regular territory reviews and account plan discussions Represent the respective country at national and international events and congresses Obey data protection law according Alexions policy and follow Alexions SOPs and compliance policies. You Will Need To Have B. A. or B. [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
[. .. ] delegated QPPV activities and maintain inspection readiness Serve as representative and point of contact for Health Authority Inspections and Internal Process Audits Requirements Doctorate degree and 2 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] years of industry pharmacovigilance experience, OR Masters degree and 4 years of industry pharmacovigilance experience, OR Bachelors degree and 6 years of industry pharmacovigilance experience, OR Associates degree and 10 years of industry pharmacovigilance experience, OR high school diploma/ GED and 12 years of industry pharmacovigilance experience Experience in signal detection, evaluation and management [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Senior PV Quality Director
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] role, youll ensure compliance, deliver quality, and drive strategic projects-overseeing key processes, collaborating with global stakeholders, and playing a crucial role in regulatory inspections. Your deep understanding [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Good Pharmacovigilance Practice (GVP) and Good Clinical Practice (GCP) safety requirements will be instrumental in upholding the highest standards of quality and compliance. This is a highly specialised, expert position focused on individual expertise, without direct line management responsibilities. The Opportunity Act as a senior quality leader for our global pharmacovigilance (PV) [. .. ] authority inspections and audits You lead confidently in a matrix environment, motivating and aligning networked teams without direct line management authority You are a strong, concise communicator and skilled stakeholder manager who uses data and digital tools to drive continuous improvement Together, well advance along the whole patient journey with the aspiration to prevent, stop and cure diseases. Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Welwyn. If you [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Senior Associate Global Safety (Local Safety Switzerland)
• Lavamünd, Kärnten
[. .. ] 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 08.09.2026 bei Jobleads gefunden
Senior Manager R D Quality Analytics Portfolio Insights
• Basel, Basel- Stadt
[. .. ] for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cancer. The Senior Manager R D Quality Analytics Portfolio Insights is a specialized R D Quality role focused on applying advanced analytics, statistical methods, and technology-enabled approaches to strengthen independent Quality oversight of clinical development, participant protection, patient safety, and regulated research activities. This position requires practical expertise in clinical and patient-safety [. .. ] indicators, thresholds, escalation criteria, and portfolio surveillance methods aligned with RBQM and Quality by Design principles. Clinical, Safety, and Research Analytics Integrate and analyze relevant clinical study, site, subject, safety, pharmacovigilance, laboratory, monitoring, audit, inspection, vendor, system, and quality data to support R D Quality oversight. Develop analytical approaches to support data-informed audit planning/ execution and identify potential patient-safety and subject-protection risks, including adverse-event under-reporting or over-reporting, unusual clinical-event patterns, protocol-compliance concerns, data-[. .. ]
Job am 07.09.2026 bei Jobleads gefunden
• 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 am 04.09.2026 bei Jobleads gefunden
Site Monitoring Lead (SML) sponsor dedicated in Germany
Führungs-/ Leitungspositionen
[. .. ] Ms) 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. Develop and support execution of corrective action plans at site and study level. [. .. ]
Job am 30.08.2026 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Abgeschlossenes Studium
Flexible Arbeitszeiten 30+ Urlaubstage
[. .. ] und gleichzeitig über den klassischen QA-Bereich hinausblicken? Sie arbeiten gerne eigenständig, übernehmen Verantwortung und schätzen ein internationales, persönliches Arbeitsumfeld mit kurzen Entscheidungswegen? Dann könnte diese Stelle als [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Quality Assurance Manager (m/w/d) bei einem internationalen Pharmaunternehmen der richtige nächste Karriereschritt für Sie sein Verantwortung für das Qualitätsmanagementsystem (QMS) sowie dessen Pflege, Weiterentwicklung und kontinuierliche Verbesserung unter Berücksichtigung von GMP, GDP und geltenden regulatorischen Anforderungen Sicherstellung einer ordnungsgemäßen Pflege und Kontrolle von SOPs sowie weiteren qualitätsrelevanten Dokumenten Überprüfung der Einhaltung [. .. ] Unterstützung bei externen Audits, Behördeninspektionen und der Qualifizierung von Lieferanten Bearbeitung von Produktqualitätsreklamationen und qualitätsbezogenen Anfragen sowie Koordination mit den jeweiligen Ansprechpartnern Unterstützung und enge Zusammenarbeit mit Regulatory Affairs und Pharmacovigilance Zusammenarbeit mit internen und externen Partnern sowie Mitwirkung an weiteren bereichsübergreifenden Projekten und Aufgaben Ihre Vorteile Unbefristete Fest- und Direkteinstellung 30 Urlaubstage Flexible Arbeitszeiten Arbeitswoche von 37.5h Transportkostenübernahme Vielfältige Aufgabenbereiche, die insbesondere in den Bereichen Qualitätssicherung, Regulatory Affairs und Pharmacovigilance zahlreiche Möglichkeiten zur fachlichen und persönlichen Weiterentwicklung bieten Ein [. .. ]
Job am 26.08.2026 bei Jobleads gefunden
Director, Business Development-CE
• Berlin
Führungs-/ Leitungspositionen
Candidates must be located in Central Europe Company Overview: Rx Logix is a global leader in
pharmacovigilance solutions, providing innovative software and expert consulting services. Our team collaborates with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Pharmacovigilance and Risk Management professionals to enhance compliance, productivity, and quality across the drug safety value chain. Dedicated to patient safety and the advancement of medical and scientific research, Rx Logix values bold, innovative thinkers. We leverage the [. .. ] our suite of solutions, to new customers and driving new business for the company in the US and Europe. Previous pharma experience and clinical trials experience is preferred. Software Sales Manager will play an important and highly visible role in liaising with key executives in the life sciences industry. One of our core values is working as a team, and we expect our sales team to live and breathe team collaboration to ensure the teams and Rx Logix success. Essential Duties [. .. ]
Job am 21.08.2026 bei Jobleads gefunden
Senior Pharmacovigilance Safety Scientist, Benefit Risk
• Berlin
[. .. ] 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. Job responsibilities Authoring and Quality review of Aggregate reports (PSURs/ PBRERs, PADERs/ Annual Reports/ ACO/ DSUR) for [. .. ] 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. #J-18808-Ljbffr 01746257 [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Medical Science Liaison Manager für Bayern/ Baden-Würtemberg
• Hannover, Niedersachsen
[. .. ] which includes collaboration with investigators and study sites. Actively collaborating with the office and fieldbased national and international Medical Affairs team. Working collaboratively with personnel in Sales, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Marketing, Clinical Research, Pharmacovigilance, Medical Communications, and other functions. Utilizing scientific resources to deliver impactful presentations in a variety of different settings. Contributing to the development of educational programs and materials. Traveling to appointments, meetings, and conferences on a frequent and regular basis, occasionally with short notice; including national and international travel. Essential background [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Senior Manager R D Quality Analytics Portfolio Insights
[. .. ] for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cancer. The Senior Manager R D Quality Analytics Portfolio Insights is a specialized R D Quality role focused on applying advanced analytics, statistical methods, and technology-enabled approaches to strengthen independent Quality oversight of clinical development, participant protection, patient safety, and regulated research activities. This position requires practical expertise in clinical and patient-safety [. .. ] indicators, thresholds, escalation criteria, and portfolio surveillance methods aligned with RBQM and Quality by Design principles. Clinical, Safety, and Research Analytics Integrate and analyze relevant clinical study, site, subject, safety, pharmacovigilance, laboratory, monitoring, audit, inspection, vendor, system, and quality data to support R D Quality oversight. Develop analytical approaches to support data-informed audit planning/ execution and identify potential patient-safety and subject-protection risks, including adverse-event under-reporting or over-reporting, unusual clinical-event patterns, protocol-compliance concerns, data-[. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Clinical Safety Manager-Pharmacovigilance/ Drug Safety
• München, Bayern
Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety
Manager to join our team in Munich. This position plays a key role [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in the pharmacovigilance process at Medpace. Working in a team to accomplish tasks and projects that are instrumental to the companys success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Manage Clinical [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Key Account Managaer-Haemtology
• Hannover, Niedersachsen
Build partnerships that bring breakthrough therapies in rare haematology to patients who need them most. Proclinical is seeking a Key Account
Manager-Haematology to join a dynamic team in Germany. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] In this role, you will focus on building and maintaining strong commercial relationships with healthcare professionals and decision-makers in hospitals to ensure access to products within key accounts. This position is ideal for someone passionate about rare diseases and biotechnology, with [. .. ] for healthcare professionals. Collaborate cross-functionally with teams such as Marketing, MSL, DLS, MACC, and account management. Maintain accurate reporting, CRM database updates, and account management records. Collect and report pharmacovigilance information in line with internal SOPs. Represent the territory in reviews, account plan discussions, and at national/ international events and congresses. Ensure compliance with data protection laws and company policies. Key Skills and Requirements Background in biotechnology or pharmaceutical sales, preferably in the orphan market, or a masters degree in [. .. ]
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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 29 offene Stellenanzeigen für Pharmacovigilance Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmacovigilance Manager Jobs?
Aktuell suchen 6 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)
- Dr. Theiss Naturwaren GmbH (1 Job)
- Novartis (1 Job)
- Gouya Insights (1 Job)
In welchen Bundesländern werden die meisten Pharmacovigilance Manager Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Manager Jobs werden derzeit in Bayern (8 Jobs), Niedersachsen (4 Jobs) und Berlin (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Manager Jobs?
Pharmacovigilance Manager Jobs gehören zum Berufsfeld Pharmazie.
