26 Jobs für Regulatory Affairs Coordinator
Stellenangebote Regulatory Affairs Coordinator Jobs
Job am 06.12.2025 bei Jobleads gefunden
• München, Bayern
Unser Kunde ist ein führendes biopharmazeutisches Unternehmen mit Sitz in München. Ihr Aufgabenbereich: Pflege der öffentlich zugänglichen und internen webbasierten
Regulatory-Seiten, Zusammenstellung von Berichten/ Übersichten, Erstellung von Präsentationen Unterstützung bei [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Textprüfungen/ Korrekturlesen (Packungsbeilagen, Verpackungsmaterial, Kennzeichnung usw. ) sowie anderen Übersetzungen Unterstützung bei Behördeneinreichungen und Berichtspflichten sowie der entsprechenden Archivierung Vorbereitung/ Pflege von Einträgen (z. B. Gelbe Liste Identa, Rote Liste) Management von Regulatory-Dienstleistern und Lieferanten Unterstützung der Abteilungsleitung bei [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Hays Professional Solutions GmbH
Label Change Coordinator (m/w/d)
• Heppenheim
Angebote von Zeitarbeitsunternehmen
[. .. ] qualitativ einwandfreie Umsetzung zu gewährleisten Sie kommunizieren mit internen Grafikern, Lohnherstellern sowie externen Vertriebspartnern und sorgen für einen reibungslosen Informationsfluss sowie effiziente Abstimmungsprozesse Zudem fungieren Sie als [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Schnittstelle zwischen Pharmakovigilanz, Regulatory Affairs, Quality und Supply Chain und stellen sicher, dass alle relevanten Anforderungen in den Labeling-Prozessen berücksichtigt werden Ihre Qualifikationen: Sie bringen ein abgeschlossenes naturwissenschaftliches oder pharmazeutisches Studium (z. ? B. Pharmazie, Biologie, Chemie, Medizinprodukte-Technologie) oder eine vergleichbare Qualifikation im Gesundheitsbereich mit Sie besitzen Erfahrung im Labeling von Arzneimitteln oder Medizinprodukten [. .. ]
Job vor 14 Tagen bei Jooble gefunden
Midas Pharma GmbH
• Ingelheim am Rhein
30+ Urlaubstage
[. .. ] und Kooperationspartnern und damit einhergehende Reisetätigkeit (national und international) Koordination und Kooperation von und mit internen, in die Supply Chains involvierten Fachabteilungen, wie z. B. : Quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Management, Business Development, Regulatory Affairs, Finished Product Development, Legal Affairs, Finance Controlling und IP-Management Mindestens 5 Jahre relevante Berufserfahrung im Supply Chain Management der pharmazeutischen Industrie Nachweisbare Erfahrungen im Management von pharmazeutischen Fertigproduktpipelines, Kenntnisse in fertigproduktrelevanten pharmaspezifischen Themen, wie Qualität, Reg. Affairs oder Produktentwicklung sind von Vorteil Sehr gute Anwenderkenntnisse in ERP Systemen, idealerweise [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Wolters Kluwer N. V.
Operations Projects Coordinator
• Soest
Wolters Kluwer is a global leader in professional information, software solutions, and services for clinicians, nurses, accountants, lawyers, and tax, finance, audit, risk, compliance, and
regulatory sectors. The Global Branding, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Communications and Marketing (GBCM) team at Wolters Kluwer is responsible for elevating the overall company narrative and bringing a consistent, strategic message to our key internal and external stakeholders. The GBCM team supports the organization globally, interacting across multiple major time zones. As part of this [. .. ] documentation, and strategic planning support. Bachelors degree in Business, Communications, Marketing, or a related field; Experience: 5+ years of experience in project management, preferably in a communications, marketing, or corporate affairs environment. Communications Expertise: Strong understanding of messaging, channels, and audience engagement, with experience shaping communication initiatives with expert-level attention to detail and deadline-oriented. Project Management Excellence: Proven ability to manage complex, cross-functional projects and drive adoption of new processes and tools. Tech-Savvy: proficient in project management [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Wolters Kluwer N. V.
• Soest
Wolters Kluwer is a global leader in professional information, software solutions, and services for clinicians, nurses, accountants, lawyers, and tax, finance, audit, risk, compliance, and
regulatory sectors. The Global Branding, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Communications and Marketing (GBCM) team at Wolters Kluwer is responsible for elevating the overall company narrative and bringing a consistent, strategic message to our key internal and external stakeholders. The GBCM team supports the organization globally, interacting across multiple major time zones. As part of this [. .. ] documentation, and strategic planning support. Bachelors degree in Business, Communications, Marketing, or a related field; Experience: 5+ years of experience in project management, preferably in a communications, marketing, or corporate affairs environment. Communications Expertise: Strong understanding of messaging, channels, and audience engagement, with experience shaping communication initiatives with expert-level attention to detail and deadline-oriented. Project Management Excellence: Proven ability to manage complex, cross-functional projects and drive adoption of new processes and tools. Tech-Savvy: proficient in project management [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Hapeko
Supply Chain Coordinator (m/w/d) in der Pharmaindustrie (Supply-Chain-Manager/in)
• Kleinmachnow
Abgeschlossenes Studium
[. .. ] der Möglichkeit, aktiv am Unternehmensaufbau mitzuwirken. Koordination und Steuerung der gesamten Importprozesse für medizinisches Cannabis Sicherstellung der regulatorischen Compliance im Bereich Betäubungsmittel Enge Zusammenarbeit mit internen Teams [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (Supply Chain, Qualität, Regulatory Affairs) Abgeschlossenes Studium mit Schwerpunkt Supply Chain, Logistik oder vergleichbare Fachrichtung Mindestens 2 Jahre Berufserfahrung im Bereich Import/ Export, Logistik oder Supply Chain Sehr gute Kommunikationsfähigkeiten in Deutsch und Englisch (mindestens C1) Moderne Arbeitsausstattung und digitale Tools Kollegiales Team und offene Unternehmenskultur Vielfältige Entwicklungsmöglichkeiten zur Leitung SCM 75130683 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Givaudan SA
• Hamburg
Betriebliche Altersvorsorge Weihnachtsgeld
[. .. ] Entschlossenheit prägen tagtäglich unsere Zukunft und beeinflussen Milliarden von Menschen positiv. Jeder Teil von dir ist eine Bereicherung für unsere Welt. Wir sind Givaudan. Human by nature. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Als Sales Project Coordinator (m/w/d) koordinierst du die vertrieblichen Abläufe im Innendienst und bist für diese dann auch verantwortlich. Du. . . verwaltest und eröffnest Projekte (Korrespondenz mit Kunden und Geschäftspartnern wie Vertretern/ Vertriebspartnern durch Organisation und Eingabe von Projektdetails in die relevanten Systeme von Givaudan) , um die Entwicklungsarbeit zu starten/ [. .. ] usw. arbeitest Angebote für unsere Kunden aus verwaltest die Kundenpreislisten bereitest Duftbeschreibungen und kleine Präsentationen vor und gibst diese an den Kunden weiter arbeitest eng mit den Abteilungen Customer Care, Regulatory Affairs, Commercial Lab, Developmen, Marketing und Pricing zusammen übernimmst die direkte Korrespondenz und Kommunikation mit Kunden schulst neue Teammitglieder in den relevanten Systemen erstellst Statistiken und Berichte Was wir uns von dir wünschen. . . eine abgeschlossene kaufmännische Ausbildung mind. 2 Jahre Berufserfahrung in einer ähnlichen Position idealerweise in der Duftstoffindustrie [. .. ]
Job am 20.01.2026 bei Jooble gefunden
INM- Leibniz- Institut für Neue Materialien gGmbH
Project Manager in Regulatory Affairs (f/m/D)
• Saarland
Work-Life-Balance
[. .. ] different technological and medical fields. Our institute develops safe-by-design concepts for responsible ELM innovation. To lead a community-driven initiative in ELMs, we seek a Project Manager in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regulatory Affairs related to biotechnology/ biomedical products (f, m, d) to develop guidelines and best practices for the development of safe and sustainable ELM-based technologies in the future. The project manager will coordinate a knowledge-exchange network that links multiple stakeholders (academic institutions, industry, consultants and regulatory agencies) and experts with [. .. ] network. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. Reporting to project coordinator, partners and funding agencies. Your profile Master s degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical [. .. ]
Job am 20.01.2026 bei Jooble gefunden
INM- Leibniz- Institut für Neue Materialien gGmbH
• Saarland
Work-Life-Balance
[. .. ] science and synthetic biology, with huge potential for sustainable innovation in different technological and medical fields. Our institute develops safe-by-design concepts for responsible ELM innovation. Project Manager [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in Regulatory Affairs related to biotechnology/ biomedical products (f, m, d) The project manager will coordinate a knowledge-exchange network that links multiple stakeholders (academic institutions, industry, consultants and regulatory agencies) and experts with interest in ELM research, innovation and regulation. This project is framed within the collaborative network Material Vital Hub, recently [. .. ] development. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. Reporting to project coordinator, partners and funding agencies. Masters degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical translation of cell [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Denk Pharma GmbH Co. KG
Coordinator (m/w/d) International Regulatory Affairs
• München
Abgeschlossene Ausbildung
Flexible Arbeitszeiten Betriebliche Altersvorsorge
Das macht die Denk Pharma: Seit 1948 ist die DENK PHARMA als Familienunternehmen in mehr als 80 Ländern tätig. Unter unserem Slogan Quality for your Health Made in Germany schaffen [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] wir für alle Kunden mit unseren Produkten Zugang zur Heilung. Als eines der wenigen Pharmaunternehmen weltweit stellen wir unseren Kunden exakt die gleichen Arznei- und [. .. ]
Job am 22.11.2025 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] and procedures. The role will have direct exposure to Senior Management and cross-functional to Finance, Front Office and other functions to ensure a consistent roll out of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the framework. Regulatory Monitoring and Change Management: Responsible for ensuring that German risk related regulations are understood and adhered to; provide oversight of local Risk projects and liaise with the Global Change function and local counterparts in Compliance, Finance and other Functions as required for the respective project. Outsourcing Controls: Monitoring and enhancement of the SLA for Risk with other Nomura entities, escalating in cases of breaches of the terms. Operational Risk Coordinator for the Risk Function including controls testing. Regulatory Liaison: Managing the relationship with the German regulators for risk related matters. Risk MI: Management of consolidated Risk MI for the entity, liaising with the global reporting teams who are responsible for the production of the reports. Production of ad-hoc reports [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Fractional Security Compliance Lead (IT GRC) - Remote
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] Manage the full lifecycle of SOC 2 Type 2 and ISO 27001 compliance programs, utilizing automation platforms like Vanta to ensure continuous control monitoring. Serve as the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] primary liaison and coordinator for external compliance auditors, managing all evidence submission and remediation timelines. Lead rapid and accurate responses to technical security questionnaires that arise during the enterprise sales due diligence process by maintaining a knowledge base Securely administer and harden core internal IT infrastructure, specifically Google Workspace and Microsoft 365/ Entra ID. [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Zürich Zuerich
Führungs-/ Leitungspositionen
[. .. ] Manage the full lifecycle of SOC 2 Type 2 and ISO 27001 compliance programs, utilizing automation platforms like Vanta to ensure continuous control monitoring. Serve as the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] primary liaison and coordinator for external compliance auditors, managing all evidence submission and remediation timelines. Lead rapid and accurate responses to technical security questionnaires that arise during the enterprise sales due diligence process by maintaining a knowledge base Securely administer and harden core internal IT infrastructure, specifically Google Workspace and Microsoft 365/ Entra ID. [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical Research Associate III (m/f/d)
• Stein, Baden- Württemberg
[. .. ] to support potential cross-border monitoring activities. Your Contribution Independently manage all phases of site activities: identification, startup, monitoring, and closeout Conduct monitoring visits in line with study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] plans and regulatory requirements Ensure compliance at investigational sites and act as the primary contact for site staff Build and maintain strong relationships with investigators and site personnel Identify risks, provide solutions, and ensure timely resolution of studyrelated issues Perform data review and verification for patient safety and protocol adherence Conduct site training, initiate visits, and support audit/ inspection readiness Collaborate with other departments such as Data Management, Clinical Operations, and Medical Affairs Support investigator and coordinator meetings, and provide training or presentations as needed Mentor junior CRAs and contribute to continuous process improvement Participate in CAPA execution, audits, and ongoing quality assurance activities Our Strength A purpose-driven Clinical Affairs team committed to quality and patient safety Onboarding and development in a structured, supportive environment Exposure [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• Hechingen, Baden- Württemberg
[. .. ] potential cross-border monitoring activities. Your Contribution Independently manage all phases of site activities: identification, start-up, monitoring, and close-out Conduct monitoring visits in line with study plans and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory requirements Ensure compliance at investigational sites and act as the primary contact for site staff Build and maintain strong relationships with investigators and site personnel Identify risks, provide solutions, and ensure timely resolution of study-related issues Perform data review and verification for patient safety and protocol adherence Conduct site training, initiate visits, and support audit/ inspection readiness Collaborate with other departments such as Data Management, Clinical Operations, and Medical Affairs Support investigator and coordinator meetings, and provide training or presentations as needed Mentor junior CRAs and contribute to continuous process improvement Participate in CAPA execution, audits, and ongoing quality assurance activities Our Strength A purpose-driven Clinical Affairs team committed to quality and patient safety Onboarding and development in a structured, supportive environment Exposure [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Project Manager in Regulatory Affairs (f/m/D)
• Kaiserslautern, Rheinland- Pfalz
Work-Life-Balance
[. .. ] different technological and medical fields. Our institute develops safe-by-design concepts for responsible ELM innovation. To lead a community-driven initiative in ELMs, we seek a Project Manager in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regulatory Affairs related to biotechnology/ biomedical products (f, m, d) to develop guidelines and best practices for the development of safe and sustainable ELM-based technologies in the future. The project manager will coordinate a knowledge-exchange network that links multiple stakeholders (academic institutions, industry, consultants and regulatory agencies) and experts with [. .. ] network. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. Reporting to project coordinator, partners and funding agencies. Your profile Master s degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
[. .. ] by a strong global network and a commitment to best-practice corporate governance. Working closely with international stakeholders, the business plays a key role in managing compliance, governance, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and corporate affairs across multiple entities and joint ventures. Based in Brisbane, the Corporate Development team partners with senior leaders locally and internationally to deliver robust governance and operational excellence. About the Role As Assistant Manager-Corporate Development, youll support corporate governance, statutory compliance, and internal controls across the organisation and its subsidiaries. [. .. ] activities, including ASIC lodgements and statutory records Coordinating Board and committee meetings, including agendas, papers, minutes, and action tracking Maintaining internal policies, procedures, registers, and governance frameworks Preparing and submitting regulatory reports, including Modern Slavery and FIRB reporting Supporting compliance programs, onboarding, training records, and internal control initiatives Preparing internal management reports and supporting broader corporate development activities About You Youre an organised, detailoriented professional with experience in corporate governance or company secretarial work. Youre confident working with multiple stakeholders and [. .. ] provide reasonable adjustments; including alternate formats to the recruitment process for individuals with disability. If you require an adjustment to be made during the recruitment process, please email our Adjustments Coordinator at or visit hoban. com. au/ adjustments for additional contact details. #J-18808-Ljbffr 78059899 [. .. ]
Job am 22.01.2026 bei Jobleads gefunden
Spezialist (w/m/d) globaler Vertriebsinnendienst-Export B. Braun Avitum
• Melsungen, Hessen
Betriebliche Altersvorsorge Jobticket
Area Sales
Coordinator (w/m/d) Innerhalb der B. Braun Avitum AG am Standort Melsungen suchen wir im Bereich Export Drittkundengeschäft für die Betreuung der Region Middle East Africa zum nächstmöglichen [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Zeitpunkt einen Area Sales Coordinator (w/m/d) . Das Team Export Third Party betreut Distributoren, die sich auf den Vertrieb von [. .. ] den Area Sales Managern wahr. Um den kontinuierlichen Ausbau der Vertriebsaktivitäten in Zusammenarbeit mit den Distributoren zu gewährleisten, nehmen Sie im internationalen Vertriebsinnendienst notwendige Abklärungen mit Schnittstellen wie Supply Chain, Regulatory Affairs, Quality Management, Marketing, Finanzen, Rechtsabteilung etc. vor. Aufgaben und Verantwortlichkeiten Sie übernehmen die Planung, Koordination und Umsetzung aller Vertriebsaufgaben für die Region Middle East Africa in enger Abstimmung mit dem Area Sales Manager Sie unterstützen bei der Steuerung der Vertriebsaktivitäten und sind zentrale Ansprechperson für den Vertriebsinnendienst in Ihrer Region [. .. ]
Job am 22.01.2026 bei Jobleads gefunden
• Zürich
Führungs-/ Leitungspositionen
[. .. ] Manage the full lifecycle of SOC 2 Type 2 and ISO 27001 compliance programs, utilizing automation platforms like Vanta to ensure continuous control monitoring. Serve as the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] primary liaison and coordinator for external compliance auditors, managing all evidence submission and remediation timelines. Lead rapid and accurate responses to technical security questionnaires that arise during the enterprise sales due diligence process by maintaining a knowledge base Securely administer and harden core internal IT infrastructure, specifically Google Workspace and Microsoft 365/ Entra ID. [. .. ]
Job am 20.01.2026 bei Jobleads gefunden
Project Manager in Regulatory Affairs (f/m/D)
• Saarbrücken, Saarland
Work-Life-Balance
[. .. ] science and synthetic biology, with huge potential for sustainable innovation in different technological and medical fields. Our institute develops safe-by-design concepts for responsible ELM innovation. Project Manager [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in Regulatory Affairs related to biotechnology/ biomedical products (f, m, d) to develop guidelines and best practices for the development of safe and sustainable ELM-based technologies in the future. The project manager will coordinate a knowledge-exchange network that links multiple stakeholders (academic institutions, industry, consultants and regulatory agencies) and experts with [. .. ] network. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. Reporting to project coordinator, partners and funding agencies. Your profile Masters degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical translation [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Clinical Research Associate III
• Berlin
[. .. ] advantage, to support potential crossborder monitoring activities. Your contribution Independently manage all phases of site activities: identification, startup, monitoring, and closeout Conduct monitoring visits in line with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] study plans and regulatory requirements Ensure compliance at investigational sites and act as the primary contact for site staff Build and maintain strong relationships with investigators and site personnel Identify risks, provide solutions, and ensure timely resolution of studyrelated issues Perform data review and verification for patient safety and protocol adherence Conduct site training, initiate visits, and support audit/ inspection readiness Collaborate with other departments such as Data Management, Clinical Operations, and Medical Affairs Support investigator and coordinator meetings, and provide training or presentations as needed Mentor junior CRAs and contribute to continuous process improvement Participate in CAPA execution, audits, and ongoing quality assurance activities Our strength A purposedriven Clinical Affairs team committed to quality and patient safety Onboarding and development in a structured, supportive environment Exposure to [. .. ]
Job am 31.10.2025 bei Jobleads gefunden
Associate Director, Global Regulatory Affairs, Advertising and Promotion
• Glattbrugg, Zürich
Führungs-/ Leitungspositionen
[. .. ] efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring lifechanging therapies to patients worldwide. The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Associate Director, Global Regulatory Affairs Advertising and Promotion (GRA A P) Review Lead is accountable for management of all assigned programs/ products as the internal expert on US and international Codes, guidance, and industry standards pertaining to prescription medicine promotion. How you will contribute: As our Associate Director, Global Regulatory Affairs Advertising and Promotion lead [. .. ] review, approval, and implementation of medical and commercial materials. You will be product or project business lead for global CMRP at Takeda CMRP Meeting Chair-pausing to communicate comments to coordinator, diffusing team disputes, serving as a dependable negotiator, keeping team focus on our ultimate stakeholders which are the patients who trust us to do the right thing, and overseeing escalation steps if MLR cannot come to alignment or if there is new data or campaigns that require senior level management [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Director Managementberatung (human)
• Düsseldorf, Nordrhein- Westfalen
Führungs-/ Leitungspositionen Beratungs-/ Consultingtätigkeiten Abgeschlossenes Studium
Flexible Arbeitszeiten
[. .. ] Beste IT Dienstleister 2024 I Wirtschaftswoche Best of Consulting Mittelstand 2022 und 2023 im Bereich Organisation und 2023 auch im Bereich Digital Transformation Deine Ansprechpartnerin für Fragen [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Anja Abdalla Team Coordinator Email schreiben Get notified about new Director jobs in Düsseldorf, North Rhine-Westphalia, Germany. Düsseldorf, North Rhine-Westphalia, Germany 1 month ago Düsseldorf, North Rhine-Westphalia, Germany 6 days ago Station Manager Assistant (m/w/d) Düsseldorf Düsseldorf, North Rhine-Westphalia, Germany 3 months ago Düsseldorf, North Rhine-Westphalia, Germany [. .. ]
Job vor 2 Tagen bei Neuvoo gefunden
Hays
Label Change Coordinator (m/w/d)
• Heppenheim, Hesse
Angebote von Zeitarbeitsunternehmen
Label Change
Coordinator (m/w/d) Arbeitnehmerüberlassung Heppenheim Startdatum: sofort Referenznummer: 859921/ 1 Diesen Job teilen oder drucken Aufgaben Sind Sie für die Organisation, Planung und Umsetzung von Labeling-Aktivitäten für verschiedene [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Produktkategorien zuständig insbesondere für Arzneimittel, Medizinprodukte sowie weitere Gesundheitsprodukte Sie erstellen und pflegen regulatorische Basistexte und stellen sicher, dass diese stets [. .. ] und qualitativ einwandfreie Umsetzung zu gewährleisten Sie kommunizierenmit internen Grafikern, Lohnherstellern sowie externen Vertriebspartnern und sorgen für einen reibungslosen Informationsfluss sowie effiziente Abstimmungsprozesse Zudem fungieren Sie als Schnittstelle zwischen Pharmakovigilanz, Regulatory Affairs, Quality und Supply Chain und stellen sicher, dass alle relevanten Anforderungen in den Labeling-Prozessen berücksichtigt werden Profil Sie bringen ein abgeschlossenes naturwissenschaftliches oder pharmazeutisches Studium (z. ? B. Pharmazie, Biologie, Chemie, Medizinprodukte-Technologie) oder eine vergleichbare Qualifikation im Gesundheitsbereich mit Sie besitzen Erfahrung im Labeling von Arzneimitteln oder Medizinprodukten idealerweise [. .. ]
Job vor 2 Tagen bei Neuvoo gefunden
IQVIA
Global Clinical Trial Coordinator (m/w/d) , German Speaking, Home-Office in Germany
• Frankfurt, Hessen
Homeoffice möglich
[. .. ] of early clinical trials. Joining our team offers the opportunity to work on innovative projects in a dynamic environment. You will support trial preparation, documentation, and coordination, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensuring compliance with regulatory standards and internal processes. This role combines operational and administrative responsibilities and requires close collaboration with internal and external stakeholders. We currently offer an exciting opportunity to join the FSP team as global Clinical Trial Coordinator ECT (m/w/d) in full-time and work home-based throughout Germany. RESPONSIBILITIES Coordinate clinical trials in early clinical development for both Sponsor and Study site. Support Clinical Trial Leaders, Clinical Trial Managers, Clinical Research Associates and Principal Investigators in all study-related activities throughout all study phases (preparation, [. .. ] documentation Compilation and collection of submission documents. Maintain trial-specific data and timelines in electronic systems. Communicate effectively with internal and external partners (e. g. , statisticians, data managers, regulatory affairs, investigators) . Organize and monitor study-related activities, meetings, and documentation. Ensure timely preparation of submission documents for authorities and ethics committees. Manage essential documents for Investigator Site File (ISF) and ensure Trial Master File (TMF) completeness and compliance. Act as TMF Records Specialist: oversee TMF strategy, perform quality checks, [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Regulatory Affairs Coordinator pro Jahr?
Als Regulatory Affairs Coordinator verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Regulatory Affairs Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 26 offene Stellenanzeigen für Regulatory Affairs Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Regulatory Affairs Coordinator Jobs?
Aktuell suchen 10 Unternehmen nach Bewerbern für Regulatory Affairs Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Regulatory Affairs Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Regulatory Affairs Coordinator Stellenangebote:
- Wolters Kluwer N. V. (2 Jobs)
- Hays Professional Solutions GmbH (1 Job)
- Midas Pharma GmbH (1 Job)
- Hapeko (1 Job)
- Givaudan SA (1 Job)
In welchen Bundesländern werden die meisten Regulatory Affairs Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Regulatory Affairs Coordinator Jobs werden derzeit in Bayern (3 Jobs), Hessen (3 Jobs) und Baden-Württemberg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Regulatory Affairs Coordinator Jobs?
Regulatory Affairs Coordinator Jobs gehören zum Berufsfeld Regulatory Affairs & Management.
