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Pharmaindustrie: 46 Jobs in Eschweiler

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  • Pharmazie 8
  • Leitung 6
  • Pharmaberater 6
  • Pharmareferent 6
  • Teamleitung 6
  • Chemie 5
  • Gruppenleitung 4
  • Sap/Erp-Beratung 3
  • Außendienst 3
  • Entwicklung 3
  • Forschung 3
  • Prozessmanagement 3
  • Labor 3
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  • Bereichsleitung 2
  • Qualitätsmanagement 2
  • Bauwesen 1
  • Betriebs- 1
  • Biologie 1
  • Business Development 1
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  • Pharmaindustrie
Berufserfahrung
  • Mit Berufserfahrung 46
  • Ohne Berufserfahrung 15
  • Mit Personalverantwortung 7
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  • Vollzeit 46
  • Home Office 3
  • Teilzeit 2
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  • Feste Anstellung 43
  • Befristeter Vertrag 3
Pharmaindustrie

Senior Medicinal Chemist (m/f/d)

Di. 27.10.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion. As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity. Join us at Grünenthal, unleash your full potential and help us change lives for the better. Job fact summary Job ID: 36995 Senior Medicinal Chemist (m/f/d) Research & Development Aachen published 08.10.2020 Senior Medicinal Chemist (m/f/d) You are accountable for discovery of high quality clinical candidates and ultimate delivery of positive Proof-of-Concept studies for innovative pain assets (by functional expertise and project leadership) You provide thought-leadership in their domain of expertise maximizing asset value You design, implement and execute medicinal chemistry strategies (small and large molecules) You create and execute medicinal chemistry plan to ensure high quality, robust and cost-effective support of company discovery portfolio You are accountable to develop strong design solutions to medicinal chemistry challenges in drug discovery You are contributing to project and department strategic planning and intellectual property protection You regularly assess developments in the field beyond classical small molecules like e.g. oligonucleotide therapeutics and identify areas for future investment relevant for drug discovery in pain You have several years of industry experience in small molecule drug discovery, including experience in other modalities like PROTAC, oligonucleotide therapeutics, etc. You have a strong track record of scientific innovation in medicinal chemistry and success in delivering high quality clinical candidates You have proven expertise in Synthetic Chemistry/ Medicinal Chemistry/ Pre-clinical Development ranging from Target Identification to PoC You have a substantial track record of innovation and milestone delivery in drug discovery projects across both early and late discovery phase and into clinical testing You have a strong knowledge in chemical biology and proven experience of when to use various chemical modalities in drug discovery You have an excellent understanding of drug discovery, various hit finding strategies, multi-parameter optimization and IP strategies You have an excellent understanding of the external CRO provider landscape
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Head Toxicology (m/f/d)

Di. 27.10.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion. As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity. Join us at Grünenthal, unleash your full potential and help us change lives for the better. Job fact summary Job ID: 36975 Head Toxicology (m/f/d) Research & Development Aachen published 08.10.2020 Head Toxicology (m/f/d) You lead the Toxicology team and are responsible for all target-based safety assessments, preclinical safety assessments and implement discovery toxicology strategies to enable the progression of optimized drug candidates You develop overall toxicology plans for lead candidates for Ph I to Ph III You provide strategic guidance for project teams and senior management including evaluation of conclusions and potential impact of toxicology results on program and clinical/ regulatory strategy You lead the development of early hypothesis-driven investigation into mechanisms of toxicity for the proactive management of potential safety liabilities and communication of impact to teams You are responsible for the safety strategy and input to multi-disciplinary drug-hunting project teams You represent Preclinical Development on Discovery and Development teams and interface with internal and external colleagues to ensure timely and accurate dissemination of nonclinical safety strategies as well as results to drive the portfolio strategically You monitor toxicology studies; review, summarize, interpret and integrate complex data sets across multiple disciplines; finalize as submission-ready documents for regulatory authorities You address and resolve scientific issues arising in drug discovery/ development programs You hold a PhD in Toxicology or closely related field with several years' experience in a drug discovery/ development setting of a biopharmaceutical company You have a proven track record of making major contributions to the discovery of one or more marketed or in-development medicines, incl. designing, monitoring, and interpreting toxicology studies to support clinical development of candidate therapeutic agents You have expert knowledge of nonclinical data packages needed to support first in human studies, clinical development and product registration You have extensive experience of regulatory toxicology/ pathology You have strategic leadership/ managerial competencies You are familiar with more than one of the following therapeutic modalities preferred: small or large molecules, cell and gene therapy You are a can-do person, problem solver who takes hands on approach to driving projects forward You have expert knowledge of GLP regulations and experience in the oversight of contracted studies
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Medical Science Liaison Manager (m/w)

Di. 27.10.2020
Köln, Kaiserslautern, Saarbrücken, Trier, Koblenz am Rhein, Bonn, Aachen
Vifor Pharma Group, formerly Galenica Group, is a global specialty pharmaceuticals company that researches, develops, produces and markets its own pharmaceutical products and is the partner of choice for innovative, patient-focused solutions. The company’s goal is to be a global leader in iron deficiency, nephrology and cardio-renal therapies and strives to help patients around the world with severe and chronic diseases to lead better, healthier lives. Vifor Pharma Group has production sites in Switzerland and Portugal as well as a dynamic network of affiliates and partners offering broad market coverage all over the world. The company has an ever-growing global presence while at the same time remaining firmly rooted in its home market, Switzerland. Vifor Pharma Group consists of Vifor Pharma; Vifor Fresenius Medical Care Renal Pharma, its joint company with Fresenius Medical Care; Relypsa; and OM Pharma. Medical Science Liaison Manager - Köln, Kaiserslautern, Saarbrücken, Trier, Koblenz, Bonn, Aachen Ort: Germany - Field based Funktion: Medical Affairs Firma: Vifor Pharma Senioritätslevel: ManagerWe are searching for a Medical Science Liaison Manager for the region Köln, Kaiserslautern, Saarbrücken, Trier, Koblenz, Bonn, Aachen. In this position, you will represent Medical Affairs externally to establish and maintain medical relationships with Key Opinion Leaders (KOLs), HCPs and key accounts on behalf of Vifor Pharma Group.  Yours tasks will include the following: Develop and maintain scientific and medical expertise (Indications and products) Identify, develop and maintain relationships with KOLs, HCPs and professional organizations KOL engagement, key account medical support, training and other appropriate activities Facilitate scientific engagement, scientific exchange and medical information Provide clinical presentations and respond to medical requests  Update medical team and other internal stakeholders on medical community interactions  Support the development, implementation and completion of medical activities (advisory boards, congress symposia, hospital meetings and speaker programs) and attend relevant scientific meetings and conferences Serves as a medical resource for internal medical and sales training Support company sponsored clinical research and IIS process  Ensure compliance with applicable local and global laws, regulations, guidelines and company policies and procedures Develop personal and professional capabilities to improve skills and professional capabilities MSc in Medical Field (e.g. Pharmacy, Chemistry or Biology)  Minimum of 3 years’ experience in research, pharmaceutical medical affairs or clinical practice Minimum of 3 years’ experience with pharma industry and healthcare compliance requirements locally and globally Demonstrated experience in KOL, HCP or medical community engagement Excellent oral and written communication skills in German and good oral and written communication skills in English Experience in public scientific presentations We are looking for a strong team player with good communication and networking skills. An entrepreneurial spirit with a humble approach and the ability to influence and persuade stakeholders are important competencies for this role.
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DMPK Scientist (m/f/d)

Di. 27.10.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion. As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity. Join us at Grünenthal, unleash your full potential and help us change lives for the better. Job fact summary Job ID: 37035 DMPK Scientist (m/f/d) Research & Development Aachen published 08.10.2020 DMPK Scientist (m/f/d) You serve as DMPK project representative on global discovery and development programs You provide metabolism and drug-drug interaction guidance to discovery project teams to mitigate issues such as “soft spot identification,” “major metabolites” to enable identification of high quality “first in man” candidates You lead the interpretation of metabolite ID studies conducted at CROs and serve as internal expert on structure elucidation, metabolic pathways and reactive metabolite formation You serve as bio-transformation subject matter expert providing expert guidance on metabolic pathways of small molecules and alternate modalities such as anti-sense oligonucleotides, peptides, etc. You demonstrate high proficiency across a wide range of in vitro/ in vivo DMPK technologies and are capable of initiating new areas of investigation that are scientifically meaningful in supporting drug discovery projects You monitor project progress with CROs and provide timely and valuable guidance to enable studies being executed appropriately You support human dose projection calculations and support clinical pharmacology trial design based on DDI risk analysis based on nonclinical data and refining based on clinical data You hold a PhD in Drug Metabolism/ Pharmacokinetics or related discipline You have demonstrated extensive experience in conducting/ managing DMPK studies (in vitro and in vivo) at CROs You have demonstrated knowledge in interpreting met-id data and proposing metabolic pathways across species You have experience or knowledge in bioanalytical methods and technologies for small molecules and biologics and in biomarker assays You have experience in working and delivering projects within highly outsourced and matrixed environments across diverse geographies and working cultures You have a proven track record in leading and working in teams based upon a matrix reporting You have a broad understanding of various DMPK relevant areas such as physicochemical properties, drug metabolizing enzyme & transporter kinetics, pharmacokinetics, mechanistic biotransformation, analytical sciences and PK/dose modelling You have strong interpersonal, communication, presentation, and negotiation skill
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Head DMPK (m/f/d)

Di. 27.10.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion. As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity. Join us at Grünenthal, unleash your full potential and help us change lives for the better. Job fact summary Job ID: 36976 Head DMPK (m/f/d) Research & Development Aachen published 08.10.2020 Head DMPK (m/f/d) You are accountable for developing DMPK strategies to build a portfolio of high quality clinical candidates, including translational PKPD understanding from non-clinical models, leading to a prediction of clinical pharmacokinetics, efficacious and tolerable dose/schedules and  potential drug-drug interaction profile and interpreting clinical studies You lead and develop DMPK team to support lead optimization, IND-enabling programs and clinical PoC You ensure in time delivery of preclinical and translational DMPK work package from early drug discovery to launch and life cycle management You establish DMPK strategies that align with program goals and strive for high quality clinical candidates You integrate CRO DMPK/PD, bioanalytical, and biotransformation data to address key issues and enable informed, timely decision making You design, manage and review CRO preclinical studies to understand  DMPK profile of candidates to influence discovery decisions and support IND-enabling studies and clinical development You drive human dose projection calculations and support clinical pharmacology trial design based on DDI risk analysis based on nonclinical data and refining based on clinical data You demonstrate high proficiency across a wide range of in vitro/ in vivo DMPK technologies and being capable of initiating new areas of investigation that are scientifically meaningful in supporting drug discovery and development programs You hold a PhD in Drug Metabolism/ Pharmacokinetics or related discipline You have several years of relevant experience in DMPK with several years of experience as a line manager in drug discovery and development with track record of taking molecules to the clinic and beyond You have a track record of developing and leading a strong scientifically data driven DMPK team to support both research and clinical stage programs You have a broad understanding of various DMPK relevant areas such as physicochemical properties, drug metabolizing enzyme & transporter kinetics, pharmacokinetics, mechanistic biotransformation, analytical sciences and PK/ dose modelling You are experienced in interpreting met-id data and proposing metabolic pathways across species You have extensive experience in managing CROs, GLP and other regulated activities You have outstanding problem-solving skills, with proven ability to integrate across disciplines to address issues and identify mitigation strategies
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Head Chemistry (m/f/d)

Di. 27.10.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion. As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity. Join us at Grünenthal, unleash your full potential and help us change lives for the better. Job fact summary Job ID: 36957 Head Chemistry (m/f/d) Research & Development Aachen published 08.10.2018 Head Chemistry (m/f/d) You provide inspirational and proactive  leadership of Drug Discovery Chemistry (Medicinal Chemistry, Synthetic Chemistry and Computational Chemistry) from lead generation through to candidate selection You are responsible for creating and executing a chemistry strategy for drug discovery that ensures the delivery of high quality clinical candidates You are accountable to provide expert functional input to create, advance and deliver a project from target idea to successful proof-of-concept clinical trial You develop strong design solutions to medicinal chemistry challenges in drug discovery You regularly assess developments in the field beyond classical small molecules like e.g. oligonucleotide therapeutics and identify areas for future investment relevant for drug discovery in pain You are responsible to monitor and optimize performance and motivation of internal and external providers to maximize output for the research programs You have several years of industry experience in small molecule drug discovery, including experience in other modalities like PROTAC, oligonucleotide therapeutics, etc. You have a strong track record of scientific innovation in medicinal chemistry and success in delivering high quality clinical candidates You have proven expertise in Synthetic Chemistry/ Medicinal Chemistry/ Pre-clinical Development ranging from target identification to PoC You have a strong knowledge in chemical biology and proven experience of when to use various chemical modalities in drug discovery You are truth seeking and delivery focused, a driven/passionate scientist with strong focus on creating value, problem solving and making things happen You are a can-do person who can take a hands on approach driving projects forward
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Senior Toxicologist (m/f/d)

Di. 27.10.2020
Aachen
Grünenthal is a global leader in pain management and related diseases. We’re driven to seek effective, life-changing medicines and solutions for patients with severe diseases and high unmet medical needs. We’re focussing all of our activities and efforts on moving towards our vision of a world free of pain. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to people living with pain worldwide. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30 countries across Europe, Latin America and the US. Our products are sold in more than 100 countries. In 2018, we employed around 4,900 people and achieved sales of € 1.3 billion. As a player in an innovative, fast-paced market, we offer an exciting working environment and wide-ranging individual development opportunities. Our shared values form the basis for the way we work: We embrace diversity, put patients at the centre of our decisions, live entrepreneurship, join forces, drive performance and act with integrity. Join us at Grünenthal, unleash your full potential and help us change lives for the better. Job fact summary Job ID: 37015 Senior Toxicologist (m/f/d) Research & Development Aachen published 08.10.2020 Senior Toxicologist (m/f/d) You lead the development and execution of toxicology, safety pharmacology, and other critical safety studies in support of Grünenthal´s R&D pipeline You develop overall toxicology plans for lead candidates for Ph I to Ph III You provide strategic guidance for project teams including evaluation of conclusions and potential impact of toxicology results on program and clinical/ regulatory strategy You lead the development of early hypothesis-driven investigation into mechanisms of toxicity for the proactive management of potential safety liabilities and communication of impact to teams You provide expert level guidance in designing and implementing preclinical toxicology studies at external contract research organizations (CRO) You monitor toxicology studies; review, summarize, interpret and integrate complex data sets across multiple disciplines; finalize as submission-ready documents for regulatory authorities You interact with regulatory authorities with in-depth knowledge on subject matter area, regulatory requirements and guidelines related to pharmacology, toxicology and nonclinical drug development in general You characterize the toxicology profile of candidate molecules and provide input into investigative studies and clinical starting dose strategies You hold a PhD in Toxicology or closely related field with several years’ experience in a drug discovery/ development setting of a biopharmaceutical company You have a proven track record of making major contributions to the discovery of one or more marketed or in-development medicines, incl. designing, monitoring, and interpreting toxicology studies to support clinical development of candidate therapeutic agents You have expert knowledge of nonclinical data packages needed to support first in human studies, clinical development and product registration You are familiar with more than one of the following therapeutic modalities preferred: small or large molecules, cell and gene therapy You have a theoretical and experimental background in pathology, biology, DMPK coupled with a solid foundation in quantitative pharmacology You have an understanding of the regulatory process including CMC, non-clinical and clinical and the various stages of drug discovery and clinical development You have expert knowledge of GLP regulations and experience in the oversight of contracted studies
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Medical Science Liaison Manager (m/w/d) – Region Mitte/West

Mo. 26.10.2020
Aachen, Düsseldorf, Köln, Koblenz am Rhein, Bonn, Kassel, Hessen
Sanofi ist ein weltweites Gesundheitsunternehmen, das Menschen bei ihren gesundheitlichen Herausforderungen unterstützt. Mit unseren Impfstoffen beugen wir Erkrankungen vor. Mit innovativen Arzneimitteln lindern wir ihre Schmerzen und Leiden. Wir kümmern uns gleichermaßen um Menschen mit seltenen Erkrankungen wie um die Millionen von Menschen mit einer chronischen Erkrankung. Mit mehr als 100.000 Mitarbeitern in 100 Ländern weltweit übersetzen wir wissenschaftliche Innovation in medizinischen Fortschritt. Wir suchen einen Medical Science Liaison Manager im Homeoffice für die Region Mitte/West (Gebiete: Aachen, Düsseldorf, Köln, Koblenz, Bonn, Kassel).Das Ziel des Medical Science Liaison ist es, medizinische Informationen über Impfstoffe von Sanofi Pasteur für Ärzte und Gesund­heits­­dienstleister zur Verfügung zu stellen und eine vertrauensvolle Zusammenarbeit aufzubauen.Identifikation, Aufbau und Aufrechterhalten solider Netzwerke und Partnerschaften mit InteressenvertreternUnterstützung der Erschließung des Marktes für Produktein­führungenAustausch mit den Country / Regional / Global Medical Affairs Teams über das EinsatzgebietUnterstützung von externen / internen Veranstaltungen durch die Auswahl von Referenten und ReferentenbriefingDurchführung und Organisation eigener Veranstaltungen  ProjektarbeitUnterstützung bei der Identifizierung geeigneter klinischer Prüfer bzw. Prüfstellen für klinische Studien und Funktion als primärer Ansprechpartner für Investigator Sponsored StudienBereitstellung von medizinischer Unterstützung und Training für die internen Mitarbeiter nach BedarfUnterstützung der anderen Funktionen in der Zusammen­arbeit mit externen Interessenvertretern in Bezug auf medizinische ThemenErfolgreicher Abschluss im Bereich Medizin, Biologie, Pharmazie, Chemie oder ein anderer biowissenschaftlicher AbschlussMindestens 3 Jahre Berufserfahrung mit wissenschaftlichem Hintergrund in den Bereichen Immunologie und der klinischen ForschungEpidemiologische Fachkenntnisse und/oder der/des Impfstoff­entwicklung/ -marktes sind von VorteilFließende Kenntnisse in Deutsch und EnglischArbeiten nach Compliance-RichtlinienArbeiten mit gängiger Computer-Software und auch grösseren Computerprogrammen sowie medientechnische FähigkeitenTeamplayerStarke Präsentations-, Kommunikations- und Verhandlungs­fähigkeitEigenständiges Arbeiten, operationelle und strategische Fähigkeiten, Neuem aufgeschlossenEin internationales Arbeitsumfeld, in dem Sie Ihre Talente entfalten und gemeinsam in einem kompetenten Team Ideen und Innovationen verwirklichen könnenEin attraktives, am Markt und Ihrer Qualifikation ausge­richtetes Vergütungspaket mit überdurchschnittlichen Sozial­leistungen (wie z. B. der betrieblichen Altersversorgung oder unserem Gesundheitsmanagement)Eine individuelle und strukturierte Einarbeitung in Ihre neuen AufgabenSie können Ihren persönlichen Karriereweg bei Sanofi gestalten und wir unterstützen und begleiten Ihre fachliche und persönliche Entwicklung zielgerichtetSanofi bietet als weltweit erfolgreiches, wachsendes Gesund­heits­unternehmen vielfältige, auch globale Karrierewege
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Manager (m/w/d) Market Access & Scientific Affairs DACH

Mo. 26.10.2020
Karlsruhe (Baden), Fürth, Bayern, Düren, Rheinland
Bencard Allergie GmbH mit Sitz in München ist ein pharmazeutisches Unternehmen, das sich sehr erfolgreich auf das zukunftsorientierte Marktsegment Allergie ausgerichtet hat. Das Unternehmen hat sich zum Ziel gesetzt, die Lebensqualität allergiekranker Menschen stetig weiter zu verbessern und die AllerGOlogie zielstrebig weiterzudenken. Hinter dem langjährigen Erfolg des Unternehmens stehen ein starkes Arzneimittelportfolio allergenspezifischer Immuntherapien, anhaltende Innovationskraft und eine werte- und wachstumsorientierte Firmenphilosophie, die auch in Zukunft gewährleisten, als kompetenter und verlässlicher Partner in der Allergologie wahrgenommen zu werden. Jetzt kommen Sie ins Spiel: Begleiten Sie uns dabei, unsere Erfolgsgeschichte aktiv mitzugestalten und unsere Marktpräsenz weiter auszubauen.Wir suchen zum nächstmöglichen Zeitpunkt zweiManager (m/w/d) Market Access & Scientific Affairs DACHRegionale Verantwortung der KV-Gebiete Bayern, Baden-Württemberg, Rheinland-Pfalz und SaarlandZusätzlich: MASA Support in der DACH RegionGesundheitspolitische sowie medizinisch-wissenschaftliche KommunikationInhaltliche Aufarbeitung, Interpretation und Darstellung von medizinisch-wissenschaftlichen Sachverhalten/Studien und gesundheitspolitischen RahmenbedingungenDefinition der relevanten Zielgruppen von Meinungsbildnern im Gesundheitswesen und deren BetreuungEinbindung von Meinungsbildnern in Projekte zu gesundheitspolitischen und medizinisch-wissenschaftlichen FragestellungenAufbau neuer KundenkontakteProfilierung des Unternehmens als kompetenter Ansprechpartner in der AllergologieBeziehungspflege zu Ärzten, kassenärztlichen Vereinigungen, Prüfstellen und KrankenkassenErschließen neuer Potentiale aufgrund eigener MarktanalysenOptimale Zusammenarbeit mit dem Außendienst sowie den Abteilungen Marketing und Medical inklusive interner Schulungen (Konzeption und Durchführung)Präsentationen und FortbildungsveranstaltungenErstellung und Platzierung redaktioneller Beiträge in relevanten FachzeitschriftenAbgeschlossenes Studium der Naturwissenschaften, Gesundheitsökonomie oder MedizinGrundkenntnisse im A-CH GesundheitssystemVorerfahrung im Bereich Pricing und ReimbursementMindestens 5 Jahre Erfahrung in der pharmazeutischen Industrie, inklusive „Big Pharma“Mindestens 2 Jahre Market Access ErfahrungGespür für gesundheitspolitische und gesellschaftliche EntwicklungenBusinessorientierte Verkäuferpersönlichkeit mit hoher Sozialkompetenz und Durchsetzungsvermögen, Teamgeist sowie einem hohen Maß an Eigenmotivation und -verantwortungKontaktfreudigkeit sowie ein überzeugendes AuftretenAusgeprägte Analysefähigkeit, Delegierungsfähigkeit sowie der Wille, in komplexen Netzwerken zu agierenSehr gute Deutsch- sowie gute EnglischkenntnisseSehr gute Kenntnisse der gängigen MS-Office-AnwendungenEinen unbefristeten Arbeitsvertrag30 Tage JahresurlaubEinen repräsentativen Firmenwagen, auch zur privaten NutzungEine Arbeit in Wohlfühlatmosphäre – jeder Mitarbeiter ist uns wichtigFlache Hierarchien – wir begegnen uns auf AugenhöheVielseitige Weiterbildungsmöglichkeiten
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Medical Science Liaison Manager (m/w/d) Fokus Infection

Mo. 26.10.2020
Düren, Rheinland, Kassel, Hessen, Karlsruhe (Baden), Fürth, Bayern
Die AstraZeneca GmbH ist die deutsche Tochtergesellschaft des britisch-schwedischen Pharmaunternehmens AstraZeneca PLC. AstraZeneca gehört mit einem Konzernumsatz von rund 24,4 Milliarden USD (2019) weltweit zu den führenden Unternehmen der forschenden Arzneimittelindustrie. Das Unternehmen entwickelt, produziert und vertreibt innovative Arzneimittel schwerpunktmäßig in den drei Therapiebereichen Onkologie, Herz-Kreislauf- und Stoffwechselerkrankungen sowie Atemwegserkrankungen. AstraZeneca agiert in über 100 Ländern und seine innovativen Medikamente werden von Millionen Patienten weltweit angewendet. Bei AstraZeneca scheuen wir uns nicht, Dinge anders anzugehen. Wir brechen die Norm und setzen Ihre Erwartungen an ein traditionelles Pharmaunternehmen zurück. Wir definieren Arbeit neu und schaffen Innovationen. Dabei haben wir stehts unsere Unternehmenswerte im Blick: wir folgen der Wissenschaft und stellen den Patienten an die erste Stelle; wir sind auf Erfolg ausgerichtet, tun das Richtige und leben Unternehmergeist. In unserer Business Unit Medical werden die Perspektiven der Medizin und der Patienten zusammengeführt, um die Wirkung unserer Medikamente vor Vermittlern, Regulatoren, Patienten und anderen medizinischen Entscheidungsträgern zu bestätigen. Aus diesem Grund beschäftigt sich die Abteilung unter anderem mit der strategischen Planung und Durchführung wissenschaftlicher Studien. Hierbei werden Patienten stets miteinbezogen, damit ihre Perspektiven in allen Bereichen des Unternehmens reflektiert werden können.Wir suchen Sie alsMedical Science Liaison Manager (m/w/d) im Indikationsbereich Infection für das Gebiet Rheinland-Pfalz, Saarland, Hessen, Baden-Württemberg, Bayern Einfluss nehmen:Verantwortlich für den Aufbau und die kompetente Weiterentwicklung von externen Experten, Referenten und medizinisch-wissenschaftlichen Zentren der betreffenden Indikationsgebiete in der Region NorddeutschlandEigenständige Konzeption, Budgetierung, Initiierung und Umsetzung überregionaler und regionaler wissenschaftlicher Projekte, u.a. FortbildungsveranstaltungenZusammenarbeit mit wissenschaftlichen Fachgesellschaften sowie Unterstützung bei internen und externen StudienprojektenTeilnahme an internationalen, nationalen und regionalen Kongressen und SymposienPlanung und Umsetzung von internen und externen Weiterbildungsprogrammen inkl. der Erstellung wissenschaftlicher PräsentationsmaterialienAktive crossfunktionale Zusammenarbeit und x-funktionales Accountmanagement Stärken beweisen:Sie haben Ihr naturwissenschaftliches Studium, bevorzugt im Bereich Medizin oder Pharmazie, erfolgreich abgeschlossenSie konnte bereits erste Erfahrungen als Medical Science Liaison Manager idealerweise im Bereich Infektiologie / Virologie sammelnEs fällt Ihnen leicht sich selbstständig in neue Indikationen und Sachverhalte einzuarbeiten und Sie überzeugen durch Ihre Umsetzungsstärke und ZielorientierungSie verfügen über ein hohes Maß an Team- und Kooperationsfähigkeit sowie exzellente Gesprächs- und Präsentationstechniken und haben Freude an der Arbeit in cross-funktionalen TeamsFließende Deutsch- und Englischkenntnisse sowie eine entsprechende Reisebereitschaft runden Ihr Profil ab. Freuen Sie sich auf:Attraktive Pipeline und innovative ProdukteIndividuelle Entwicklungsmöglichkeiten in einem dynamischen ArbeitsumfeldVertrauen, Wertschätzung und Raum für MitgestaltungFlexible Arbeitszeitmodelle sowie ein attraktives Benefit-PaketEin agiles Team mit breiter kollegiale Unterstützung und täglichem LernenEin Unternehmen, das Nachhaltigkeit und Umweltschutz in den Fokus hat
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