24 Jobs für Pharmacovigilance Officer
Stellenangebote Pharmacovigilance Officer Jobs
Job am 24.12.2025 bei Neuvoo gefunden
Merz Therapeutics
• Frankfurt, Hessen
Abgeschlossenes Studium
Jobticket Work-Life-Balance
Pharmacovigilance Officer (m/w/d) Global Product Safety View job here Pharmacovigilance Officer (m/w/d) Global Product Safety Vollzeit Alfred-Wegener-Straße 2, 60438 Frankfurt am Main, Deutschland Mit Berufserfahrung 24.02.26 IHRE AUFGABE Als Pharmacovigilance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Officer (m/w/d) sind Sie Teil unseres Global Product Safety-Teams und tragen [. .. ]
Job am 06.02.2026 bei StepStone gefunden
Dr. Falk Pharma GmbH
Head of Global Safety Product Leads-Risk Label Management (m/f/d)
• 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 activities including preparation and review of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term use, abuse or counterfeit drugs Medical/ scientific assessment of [. .. ]
Job am 04.02.2026 bei StepStone gefunden
Dr. Falk Pharma GmbH
• Freiburg
Homeoffice möglich
[. .. ] medical progress can only be achieved by working together. That is why we are looking for: Your tasks Supporting the Head of Global Safety QPPV Office/ EU [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including: Management of safety operations incl. corresponding service providers, creation and maintenance of reporting rules (in collaboration with the department Global Safety Application Management) and license partner obligations with respective compliance outputs (e. g. KPIs, PSMF) Collection, systematic documentation and evaluation of all necessary information in connection with indications [. .. ]
Job gestern bei Mindmatch.ai gefunden
Octapharma
Lead Expert Quality Assurance, Deputy Responsible Person 40
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] for the administrative market release. Acting as interface between Swissmedic and the Corporate Regulatory Department to organise new/maintain existing Marketing Authorisations of the products. Fulfilling the required [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] tasks in Pharmacovigilance as Deputy Local Drug Safety Officer for Switzerland/Liechtenstein. Giving support in various Quality Assurance tasks (e. g. Document Management System, internal auditing, employee training, Gx P tasks like handling of change controls, deviations, CAPA, returns, PQR review, qualification of service providers, etc. ) . During the absence of the Responsible Person and where immediate action is [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
F. Hoffmann- La Roche AG
• AT- 9 Wien
[. .. ] , and Risk Enablers. Identify local data gaps and lead data generation activities; design and oversee Post-Market Clinical Follow-Up (PMCF) plans and studies. Serve as a Study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Safety Officer for assigned clinical trials, ensuring the well-being of participants and the integrity of study data. Serve as MRA author for assays, IVDs and laboratory products. Stakeholder Engagement Scientific Exchange: Develop and cultivate robust, long-term strategic relationships with internal colleagues, clinicians, research institutions, and other key external stakeholders in [. .. ] state-of-the-art. Demonstrated experience in developing and managing relationships with teams and experts in the Diabetes or related space. Strong understanding of clinical trial design, data analysis, and pharmacovigilance/ device safety. Experience with clinical trial safety oversight as a Study Safety Officer is a significant asset. Strategic mindset with the ability to translate complex scientific and technical concepts into actionable plans. Excellent communication, presentation, and interpersonal skills. A true team player is a must. Fluency in English is required. [. .. ]
Job vor 14 Tagen bei Mindmatch.ai gefunden
Roche
Senior Clinical Evaluation Manager (m/f/d)
• AT- 9 Wien
[. .. ] , and Risk Enablers Identify local data gaps and lead data generation activities; design and oversee Post-Market Clinical Follow-Up (PMCF) plans and studies Serve as a Study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Safety Officer for assigned clinical trials, ensuring the well-being of participants and the integrity of study data Serve as MRA author for assays, IVDs and laboratory products Stakeholder Engagement Scientific Exchange: Develop and cultivate robust, long-term strategic relationships with internal colleagues, clinicians, research institutions, and other key external stakeholders in [. .. ] state-of-the-art Demonstrated experience in developing and managing relationships with teams and experts in the Diabetes or related space Strong understanding of clinical trial design, data analysis, and pharmacovigilance/ device safety Experience with clinical trial safety oversight as a Study Safety Officer is a significant asset Strategic mindset with the ability to translate complex scientific and technical concepts into actionable plans Excellent communication, presentation, and interpersonal skills A true team player is a must Fluency in English is required. [. .. ]
Job am 09.02.2026 bei Mindmatch.ai gefunden
F. Hoffmann- La Roche Gruppe
• AT- 9 Wien
[. .. ] , and Risk Enablers. Data gaps PMCF: Identify local data gaps and lead data generation activities; design and oversee Post-Market Clinical Follow-Up (PMCF) plans and studies. Study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Safety Officer: Serve as a Study Safety Officer for assigned clinical trials, ensuring participant safety and data integrity. MRA authoring: Serve as MRA author for assays, IVDs and laboratory products. Stakeholder Engagement Scientific Exchange: Develop and cultivate robust, long-term strategic relationships with internal colleagues, clinicians, research institutions, and external stakeholders in [. .. ] for medical devices) ; solid understanding of Diabetes and CGM technologies; ability to manage relationships with Diabetes-focused experts. Clinical safety knowledge: Strong understanding of clinical trial design, data analysis, pharmacovigilance/ device safety; experience as Study Safety Officer is an asset. Communication teamwork: Excellent communication, presentation, and interpersonal skills; true team player; fluent in English; German proficiency is highly advantageous. In Austria, we disclose the minimum salary according to our collective agreement: gross EUR 3, 843 per month for this position. [. .. ]
Job am 08.02.2026 bei Mindmatch.ai gefunden
F. Hoffmann- La Roche AG
Senior Medical Manager/ Senior Clinical Evaluation Manager
• AT- 9 Wien
[. .. ] , and Risk Enablers. Identify local data gaps and lead data generation activities; design and oversee Post-Market Clinical Follow-Up (PMCF) plans and studies. Serve as a Study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Safety Officer for assigned clinical trials, ensuring the well-being of participants and the integrity of study data. Serve as MRA author for assays, IVDs and laboratory products. Stakeholder Engagement Scientific Exchange: Develop and cultivate robust, long-term strategic relationships with internal colleagues, clinicians, research institutions, and other key external stakeholders in [. .. ] state-of-the-art. Demonstrated experience in developing and managing relationships with teams and experts in the Diabetes or related space. Strong understanding of clinical trial design, data analysis, and pharmacovigilance/ device safety. Experience with clinical trial safety oversight as a Study Safety Officer is a significant asset. Strategic mindset with the ability to translate complex scientific and technical concepts into actionable plans. Excellent communication, presentation, and interpersonal skills. A true team player is a must. Fluency in English is required. [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Genf
[. .. ] under the supervision of the Legal Counsel Lead. These agreements include in particular clinical trial related agreements (incl. service agreements with investigators, CROs, laboratories) collaboration agreements, technical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] agreements (quality and pharmacovigilance) and research agreements. Conduct legal research on intellectual property matters of importance to the organisation and assist the Legal Counsel Lead in the management of GARDP trademarks portfolio. Contribute to the corporate housekeeping of GARDP Foundation. Liaise with relevant departments to ensure that legal risks have been identified and advise [. .. ] legal matters. Perform any other relevant duties assigned by the General Counsel. Main Interactions Work closely with the other members of the legal team (General Counsel, Legal Counsel Lead, Paralegal Officer and Legal Consultants) Support colleagues from other departments (Business Development, Global Access, Research Development, Internal Operations (incl. IT, Finance, HR, Procurement) , External Affairs (incl. External Relations, Communication) and Executive Office) Others Travel requirements: max. 5 Demonstrate common sense and be articulate, proactive, solution-oriented, rigorous and have a strategic [. .. ]
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 activities including preparation and review of study-specific documents Pharmacovigilance obligations and roles Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term use, abuse or counterfeit drugs Medical/ scientific assessment of [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Senior Clinical Evaluation Manager (m/f/d)
• Wien
Beratungs-/ Consultingtätigkeiten
[. .. ] , and Risk Enablers Identify local data gaps and lead data generation activities; design and oversee Post-Market Clinical Follow-Up (PMCF) plans and studies Serve as a Study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Safety Officer for assigned clinical trials, ensuring the well-being of participants and the integrity of study data Serve as MRA author for assays, IVDs and laboratory products Stakeholder Engagement Scientific Exchange: Develop and cultivate robust, long-term strategic relationships with internal colleagues, clinicians, research institutions, and other key external stakeholders in [. .. ] state-of-the-art Demonstrated experience in developing and managing relationships with teams and experts in the Diabetes or related space Strong understanding of clinical trial design, data analysis, and pharmacovigilance/ device safety Experience with clinical trial safety oversight as a Study Safety Officer is a significant asset Strategic mindset with the ability to translate complex scientific and technical concepts into actionable plans Excellent communication, presentation, and interpersonal skills A true team player is a must Fluency in English is required. [. .. ]
Job am 08.02.2026 bei Jobleads gefunden
Senior Medical Manager/ Senior Clinical Evaluation Manager
• Wien
[. .. ] , and Risk Enablers. Identify local data gaps and lead data generation activities; design and oversee Post-Market Clinical Follow-Up (PMCF) plans and studies. Serve as a Study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Safety Officer for assigned clinical trials, ensuring the well-being of participants and the integrity of study data. Serve as MRA author for assays, IVDs and laboratory products. Stakeholder Engagement Scientific Exchange: Develop and cultivate robust, long-term strategic relationships with internal colleagues, clinicians, research institutions, and other key external stakeholders in [. .. ] state-of-the-art. Demonstrated experience in developing and managing relationships with teams and experts in the Diabetes or related space. Strong understanding of clinical trial design, data analysis, and pharmacovigilance/ device safety. Experience with clinical trial safety oversight as a Study Safety Officer is a significant asset. Strategic mindset with the ability to translate complex scientific and technical concepts into actionable plans. Excellent communication, presentation, and interpersonal skills. A true team player is a must. Fluency in English is required. [. .. ]
Job am 07.02.2026 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] access enablers and reputation metrics Provide external intelligence and ecosystem insight to senior leadership and cross-functional teams Partner closely with Medical, Market Access, Commercial, HEOR, Regulatory, Legal, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Compliance and Pharmacovigilance Ensure excellence in governance, ethics and compliance across all external engagements You will combine strategic vision, operational excellence and executive presence. Your Profile You Bring 810+ years of experience in healthcare public affairs, patient advocacy and communications Very good understanding of healthcare environment in Germany Knowledge of the area of [. .. ] of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incytes data protection officer, and your supervisory authority (if applicable) . Please contact if you have any questions or concerns or would like to exercise your rights. #J-18808-Ljbffr 79766546 [. .. ]
Job am 07.02.2026 bei Jobleads gefunden
Chief Medical Officer
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] company focused on developing innovative therapies for patients with solid tumours. With an advancing pipeline spanning Phase I to Phase III clinical development, we are seeking an [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accomplished Chief Medical Officer (CMO) to lead our global clinical and medical strategy. Reporting directly to the CEO, the CMO will be a key member of the executive leadership team and will play a central role in regulatory success, late-stage development, and value creation. Responsibilities Define and execute the overall clinical development and [. .. ] Phase meetings, and marketing authorisation procedures. Serve as the primary medical representative in regulatory meetings, advisory committees, and interactions requiring expert medical judgment and credibility. Oversee clinical operations, medical monitoring, pharmacovigilance, and safety governance. Partner closely with Regulatory Affairs to shape regulatory strategy, briefing documents, and responses to agency questions. Engage and manage relationships with key investigators, KOLs, academic collaborators, and advisory boards. Represent the company externally at major scientific congresses, partnering discussions, and investor presentations. Build, lead, and mentor a [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
• Morges, Waadt
Führungs-/ Leitungspositionen
[. .. ] discovery organization, regulatory and others. Provides medical and scientific expertise for internal cross-functional team members for development of specific, hematology-oncology agents including discovery scientists, clinical scientists, biostatisticians, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] pharmacokinetics, pharmacovigilance, and clinical operations. Supports interactions with global regulatory bodies including the FDA, EMA, PMDA and TGA and ethics committees to accomplish tasks related to product development and collaborates with internal regulatory experts and oversee the clinical research plans and sections for Investigational new Drug applications (INDs) and other regulatory documents. [. .. ] of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incytes data protection officer, and your supervisory authority (if applicable) . Please contact if you have any questions or concerns or would like to exercise your rights. Seniority level Director Employment type Full-time Job function Research Industries Pharmaceutical Manufacturing #J-18808-Ljbffr 71927131 [. .. ]
Job am 27.09.2025 bei Jobleads gefunden
Global head of pharmacovigilance
• Thüringen
Führungs-/ Leitungspositionen
[. .. ] central to ensuring safe, compliant, and successful oncology drug development and to maximising patient safety from clinical trials to post-marketing surveillance. This position will report to the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Chief Medical Officer and either work on a hybrid basis from the company office in Germany or on a remote basis. Your mission Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory requirements, especially for oncology assets. Oversee safety surveillance, signal detection, risk assessment, and risk mitigation for investigational and marketed oncology products. Ensure compliance with international PV regulations (FDA, EMA, ICH) , SOPs, and best industry practices. Lead and build high-performing PV [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
Octapharma
• Springe, Lower Saxony
Führungs-/ Leitungspositionen
[. .. ] for the administrative market release. Acting as interface between Swissmedic and the Corporate Regulatory Department to organize new/maintain existing Marketing Authorizations of the products. Fulfilling the required [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] tasks in Pharmacovigilance as Deputy Local Drug Safety Officer for Switzerland/Liechtenstein. Giving support in various Quality Assurance tasks (eg. Document Management System, internal auditing, employees training, Gx P tasks like handling of change controls, deviations, CAPA, returns, PQR review, qualification of service providers, etc. ) . During the absence of the Responsible Person and where immediate action is required, [. .. ]
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 activities including preparation and review of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term use, abuse or counterfeit drugs Medical/ scientific assessment of [. .. ]
Job am 06.02.2026 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 of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Ensuring the required quality of pharmacovigilance data Responsibility as Deputy Graduated Plan Officer according to 63a AMG which includes the following in absence [. .. ]
Job am 06.02.2026 bei Jooble gefunden
Dr. Falk Pharma GmbH
Product Marketing Manager (a)
• 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 of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Ensuring the required quality of pharmacovigilance data Responsibility as Deputy Graduated Plan Officer according to 63a AMG which includes the following in absence [. .. ]
Job am 06.02.2026 bei Jooble gefunden
Dr. Falk Pharma GmbH
Global Product Marketing Manager
• 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 of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Medical/ scientific assessment of drug risks and their documentation, taking into account the statutory reporting obligations to the competent authorities Ensuring the required quality of pharmacovigilance data Responsibility as Deputy Graduated Plan Officer according to 63a AMG which includes the following in absence [. .. ]
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 activities including preparation and review of study-specific documents Supporting the Head of Global Safety/ EU/ UK QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including Collection, systematic documentation and evaluation of all necessary information in connection with indications of drug risks, in particular adverse drug reactions, interactions and contraindications, as well as indications of quality defects, misuse, long-term use, abuse or counterfeit drugs Medical/ scientific assessment of [. .. ]
Job am 05.02.2026 bei Jooble gefunden
Incyte Corporation
Director, Public Affairs, Inflammation Autoimmunity (m/f/d)
• München
Führungs-/ Leitungspositionen
[. .. ] access enablers and reputation metrics Provide external intelligence and ecosystem insight to senior leadership and cross-functional teams Partner closely with Medical, Market Access, Commercial, HEOR, Regulatory, Legal, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Compliance and Pharmacovigilance Ensure excellence in governance, ethics and compliance across all external engagements You will combine strategic vision, operational excellence and executive presence. Your Profile You bring: 810+ years of experience in healthcare public affairs, patient advocacy and communications Very good understanding of healthcare environment in Germany Knowledge of the area of [. .. ] of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incytes data protection officer, and your supervisory authority (if applicable) . Please contact if you have any questions or concerns or would like to exercise your rights. 79481621 [. .. ]
Job am 04.02.2026 bei Jooble gefunden
Dr. Falk Pharma GmbH
Global Safety Project Manager-Operations Compliance (m/f/d)
• Regierungsbezirk Freiburg
[. .. ] medical progress can only be achieved by working together. That is why we are looking for: Your tasks Supporting the Head of Global Safety QPPV Office/ EU [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] QPPV/ Graduated Plan Officer in the fulfillment of pharmacovigilance obligations, including: Management of safety operations incl. corresponding service providers, creation and maintenance of reporting rules (in collaboration with the department Global Safety Application Management) and license partner obligations with respective compliance outputs (e. g. KPIs, PSMF) Collection, systematic documentation and evaluation of all necessary information in connection with indications [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Pharmacovigilance Officer pro Jahr?
Als Pharmacovigilance Officer verdient man zwischen EUR 60.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmacovigilance Officer Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 24 offene Stellenanzeigen für Pharmacovigilance Officer Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmacovigilance Officer Jobs?
Aktuell suchen 8 Unternehmen nach Bewerbern für Pharmacovigilance Officer Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmacovigilance Officer Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmacovigilance Officer Stellenangebote:
- Dr. Falk Pharma GmbH (8 Jobs)
- Octapharma (2 Jobs)
- F. Hoffmann- La Roche AG (2 Jobs)
- Roche (1 Job)
- F. Hoffmann- La Roche Gruppe (1 Job)
- Merz Therapeutics (1 Job)
In welchen Bundesländern werden die meisten Pharmacovigilance Officer Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Officer Jobs werden derzeit in Niedersachsen (5 Jobs), Baden-Württemberg (2 Jobs) und Hessen (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Officer Jobs?
Pharmacovigilance Officer Jobs gehören zum Berufsfeld Pharmazie.
