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Clinical affairs manager • wendlingen am neckar

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Clinical Site Manager

Clinical Site Manager

PharmiwebStuttgart, DE
As Clinical Site Manager you will be responsible for maximizing site performance and site engagement in our client conducted clinical studies, as well as leveraging strong clinical operational and ...Mehr anzeigenZuletzt aktualisiert: vor 15 Tagen
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Manager Regulatory Affairs – Head of Product Stewardship (m / f / d)

Manager Regulatory Affairs – Head of Product Stewardship (m / f / d)

BYK-Chemie GmbHStuttgart, DE
Über unsAbout us We are ALTANA : one group of companies – four divisions : BYK, ECKART, ELANTAS, and ACTEGA.Global leader in specialty chemicals with about 8,000 employees, sales of more than 2.Would...Mehr anzeigenZuletzt aktualisiert: vor 2 Tagen
Director Clinical & Medical (Medical Devices) (gn) (gn)

Director Clinical & Medical (Medical Devices) (gn) (gn)

Vality One Recruitment GmbHStuttgart, Baden-Württemberg, Germany
Quick Apply
Abteilung für Clinical Operations & Medical Affairs.Zeitmanagement, Budget und Ressourcenzuweisung.Fortschritt der klinischen Studien an die Geschäftsleitung. Zusammenarbeit mit Meinungsführern...Mehr anzeigenZuletzt aktualisiert: vor 27 Tagen
Healthcare Policy and Advocacy Manager (d / f / m) - Germany

Healthcare Policy and Advocacy Manager (d / f / m) - Germany

EssityStuttgart , Germany
Vollzeit
Healthcare Policy and Advocacy.Essity is a leading global hygiene and healthcare company.We are committed to improving the quality of life through high-quality hygiene and healthcare solutions.We s...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Senior Regulatory Affairs Expert (w / m / d) -Großraum Düsseldorf

Senior Regulatory Affairs Expert (w / m / d) -Großraum Düsseldorf

Dr. Heimeier Executive SearchStuttgart, BW
Unser Klient ist ein mittelständischer Spezialist in der chemischen Industrie und gehört zu einem international operierenden Konzern. Als eigenständig agierendes, deutsches Tochterunternehmen produz...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Medical Affairs Specialist (m / w / d)

Medical Affairs Specialist (m / w / d)

Kardion GmbHStuttgart, DE
Vorbereitung und Pflege von Studienmaterialien, Studiendokumenten sowie regulatorischen und präklinischen Dokumenten.Koordination und Durchführung von präklinischen Studien.Literaturrecherche, Ausa...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Sachbearbeiter Produktsicherheit / Gefahrstoffmanagement | Regulatory Affairs Assistant (m / w / d)

Sachbearbeiter Produktsicherheit / Gefahrstoffmanagement | Regulatory Affairs Assistant (m / w / d)

RemsgoldWinterbach, DE
Hygiene mit MEHRWERT ist unser Leitbild.In Großküchen sorgen wir mit unserem Hygienekonzept, bestehend aus Produkten, Technik und Service, für hohe Hygiene- und Sicherheitsstandards.Einen vielseiti...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Regulatory Affairs Manager - REACH (m / w / d)

Regulatory Affairs Manager - REACH (m / w / d)

HaysBaden-Württemberg
Regulatory Affairs Manager - REACH.Festanstellung durch unseren Kunden Baden-Württemberg Startdatum : sofort Referenznummer : 768787 / 1. Diesen Job teilen oder drucken.Sie unterstützen und verteidigen ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Principal Medical Science Liaison (Rare Disease / Oncology) - Southern Germany

Principal Medical Science Liaison (Rare Disease / Oncology) - Southern Germany

EVERSANAStuttgart, BW, DE
The Principal Medical Science Liaison will be responsible for establishing, developing, and maintaining relationships with key stakeholders within a defined territory. The product launch is ongoing ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
(Senior) Manager, Medical Science Liaison, Therapy Development, Transcatheter Mitral and Tricuspid Therapies (Germany)

(Senior) Manager, Medical Science Liaison, Therapy Development, Transcatheter Mitral and Tricuspid Therapies (Germany)

Edwards LifesciencesGermany, Baden, Wuerttemberg, Remote
Homeoffice
Vollzeit
Innovation starts from the heart.At Edwards, we put patients first.We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical inn...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Medical Science Liaison Manager (m / w / d) Neurologie - Region Süddeutschland

Medical Science Liaison Manager (m / w / d) Neurologie - Region Süddeutschland

Merz TherapeuticsStuttgart, Baden-Württemberg, Germany
Quick Apply
Medical Science Liaison Manager (m / w / d) Neurologie - Region Süddeutschland.Medical Science Liaison Manager (m / w / d) Neurologie - Region Süddeutschland. Medical Science Liaison Manager (m / w / d) Neurolo...Mehr anzeigenZuletzt aktualisiert: vor 2 Tagen
Regulatory Affairs Manager (m / w / d)

Regulatory Affairs Manager (m / w / d)

Polymedics Innovations GmbHKirchheim unter Teck, Baden-Württemberg, DE
Diese Tätigkeiten liegen in Ihrer Verantwortung.Erstellung und Aktualisierung der Technischen Dokumentation.Schwerpunkt USA : Strategie, Koordination, Erstellung und Einreichung.Kommunikation mit Be...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Key Account Manager Onkologie

Key Account Manager Onkologie

Inizio EngageStuttgart, DE
Stellenanzeige : Key Account Manager (m / w / d).Unser Kunde, ein europäisches Pharmazieunternehmen, gehört weltweit zu den führenden pharmazeutischen Unternehmen in der Erforschung und Entwicklung inno...Mehr anzeigenZuletzt aktualisiert: vor 9 Tagen
Regulatory Affairs Specialist (m / w / d)

Regulatory Affairs Specialist (m / w / d)

ProclinicalBaden-Württemberg, Germany
Unbefristet
Regulatory Affairs Specialist (m / w / d) - D.Erstellung und Pflege der technischen Dokumentation für Medizinprodukte gemäß MDR 2017 / 745. Sicherstellung der Einhaltung relevanter regulatorischer Vorgabe...Mehr anzeigenZuletzt aktualisiert: vor 22 Tagen
Volontariat im Bereich Communications & Public Affairs

Volontariat im Bereich Communications & Public Affairs

RocheWurttemberg, Germany
Vollzeit
Als Abteilung Communications & Public Affairs arbeiten wir gemeinsam daran, aus den vielfältigen Inhalten unseres Unternehmens spannende Geschichten zu entwickeln und diese mit kreativen Ideen und ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Pflicht-Praktikum im Bereich External Affairs, Political Operations ab September 2025

Pflicht-Praktikum im Bereich External Affairs, Political Operations ab September 2025

Mercedes-Benz Group AGStuttgart, Deutschland
Life is always about becoming… Im Leben geht es darum, sich auf eine Reise zu begeben, um die beste Version unseres zukünftigen Selbst zu werden. Während wir Neues entdecken, stellen wir uns Herausf...Mehr anzeigenZuletzt aktualisiert: vor 9 Stunden
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Pflicht-Praktikum im Bereich External Affairs, Political Operations ab September 2025

Pflicht-Praktikum im Bereich External Affairs, Political Operations ab September 2025

Mercedes-BenzStuttgart, DE
Tätigkeitsbereich : Konzernentwicklung / -strategieFachabteilung : National OperationsGesellschaft : Mercedes-Benz Group AGStandort : Mercedes-Benz Group AG Zentrale, StuttgartStartdatum : .Stellennummer : MER...Mehr anzeigenZuletzt aktualisiert: vor 20 Stunden
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Clinical Site Manager

Clinical Site Manager

PharmiwebStuttgart, DE
Vor 15 Tagen
Stellenbeschreibung

As Clinical Site Manager you will be responsible for maximizing site performance and site engagement in our client conducted clinical studies, as well as leveraging strong clinical operational and therapeutic expertise to support execution of the clinical studies.

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success.

What you will be doing :

  • Responsible for the planning, initiation, coordination and management of all monitoring and monitoring-related activities as well as supervision of all site-related activities to ensure compliance with the client Standard Operating Procedures (SOPs), Good Clinical Practices (GCP) and regulatory requirements
  • Engage with clinical sites to develop, build, and maintain strong relationships with investigators / staff that will ensure high quality investigative sites to support the client’s clinical development programs
  • Collaborate with internal and external stakeholders as well as third party vendors
  • Provide operational support to the CPM / Sr CPM to deliver the study within planned timelines and according to required standards of quality and compliance
  • Evaluate, screen and develop high quality investigative sites to support the client’s clinical development programs
  • Responsible for the early engagement with Key Opinion Leaders (KOLs) / sites / patients organizations and key contact point for these throughout the study.
  • Interact / train new investigators to work on the client clinical trials
  • Attend key therapeutic trainings / meetings and / or industry trainings

You are :

  • A SCRA with a minimum of 4+ years of monitoring experience in Germany
  • Excellent verbal and written communication in German and English
  • Operate effectively within an international and rapidly changing environment
  • Ability to monitor across Germany and supervise related activities in a clinical trial
  • Ability to have scientific discussions with Investigators and Site Personnel
  • BA / BS Degree required
  • Ability to travel domestically
  • What ICON can offer you :

    Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

    In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

    Our benefits examples include :

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
  • Visit our careers website to read more about the benefits of working at ICON : https : / / careers.iconplc.com / benefits

    ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

    If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here .

    Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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