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Clinical affairs manager • edingen neckarhausen

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(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
  • Gesponsert
Strategy Development Lead

Strategy Development Lead

Archer Daniels MidlandHeidelberg, Baden-Württemberg, Germany
In the Regulatory & Scientific Affairs (RSA) EMEA Department.Start date : As soon as possible.You lead disciplinary : You motivate and develop employees according to their needs (including determ...Mehr anzeigenZuletzt aktualisiert: vor 5 Tagen
Clinical Supplies Project Associate (m / w / d)

Clinical Supplies Project Associate (m / w / d)

BrunelMannheim, Deutschland
Sie unterstützen die Clinical Supplies Project Manager (CSPM) bei der Bereitstellung und Koordination von klinischen Prüfmustern für globale klinische Studien (Phase 1 bis 4).Sie fungieren als zent...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
Praktisches Jahr Pharmazie im Bereich Clinical Supply Pharmacy

Praktisches Jahr Pharmazie im Bereich Clinical Supply Pharmacy

AbbVieLudwigshafen am Rhein, Rhineland-Palatinate, Germany
Praktisches Jahr Pharmazie im Bereich Clinical Supply Pharmacy.AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the m...Mehr anzeigenZuletzt aktualisiert: vor 5 Tagen
Regulatory Affairs Manager (m / w / d)

Regulatory Affairs Manager (m / w / d)

Canopy GrowthHeidelberg, Baden-Württemberg
Vollzeit
Die Canopy Growth Germany GmbH, Teil der börsennotierten kanadischen Canopy Growth Corporation, ist eines der führenden Cannabisunternehmen in Deutschland. Langjährige Erfahrung, wissenschaftliche E...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
Communication & Public Affairs Manager (m / w / d)

Communication & Public Affairs Manager (m / w / d)

PHOENIX Pharmahandel GmbH & Co KGMannheim
Communication & Public Affairs Manager (m / w / d).In der PHOENIX Pharmahandel GmbH & Co KG ist ab sofort die Stelle eines Communication & Public Affairs Managers (m / w / d) zu besetzen.Unterstützung bei ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Talent pool - Germany

Talent pool - Germany

Ascendis PharmaHeidelberg, BW, DE
Quick Apply
We have locations in Denmark, Germany, the United States, the UK, Italy, Spain, and France.Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platfor...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
  • Gesponsert
  • Neu!
Regulatory Specialist (m / w / d)

Regulatory Specialist (m / w / d)

ADM WILD Europe GmbH & Co. KGEppelheim bei Heidelberg
Bereich Regulatory & Scientific Affairs.ADM nutzt die Schätze der Natur, um Menschen weltweit den Zugang zu Nahrung zu ermöglichen. Mit wegweisenden Innovationen, unserem umfassenden Portfolio an Zu...Mehr anzeigenZuletzt aktualisiert: vor 19 Stunden
  • Gesponsert
DACH Medical Director

DACH Medical Director

IQVIAMannheim, Baden-Württemberg, Germany
IQVIA is seeking a highly skilled and motivated DACH Medical Director to lead the prelaunch medical engagement activities for a groundbreaking treatment in Osteogenesis Imperfecta (OI) across the D...Mehr anzeigenZuletzt aktualisiert: vor 5 Tagen
  • Gesponsert
Regulatory Affairs Coordinator (m / w / d)

Regulatory Affairs Coordinator (m / w / d)

Thor GmbHSpeyer
Unternehmensprofil : Die THOR GmbH mit Sitz in Speyer ist Teil eines international agierenden Konzerns.An unserem Standort beschäftigen wir derzeit 700 Mitarbeiterinnen und Mitarbeiter.Schwerpunkte d...Mehr anzeigenZuletzt aktualisiert: vor 15 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
  • Gesponsert
Clinical Trials Assistant Neuropsychology

Clinical Trials Assistant Neuropsychology

The Florey Institute of Neuroscience and Mental HealthHeidelberg, Baden-Württemberg, Germany
Salary packaging of up to $18500 p.The role of the Clinical Trials Assistant (CTA) is as a participant facing representative of the Australian Epilepsy Project (AEP) central team within the Florey....Mehr anzeigenZuletzt aktualisiert: vor 4 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
  • Gesponsert
Manager Regulatory Affairs – Head of Product Stewardship (m / f / d)

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

BYK-Chemie GmbHHeidelberg, 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
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  • Neu!
Regulatory Affairs Coordinator (m / w / d)

Regulatory Affairs Coordinator (m / w / d)

THOR GmbHSpeyer
Die THOR GmbH mit Sitz in Speyer ist Teil eines international agierenden Konzerns.An unserem Standort beschäftigen wir derzeit 700 Mitarbeiterinnen und Mitarbei­ter. Schwerpunkte der Unterneh­mensak...Mehr anzeigenZuletzt aktualisiert: vor 19 Stunden
Praktikum Regulatory & Scientific Affairs (m / w / d)

Praktikum Regulatory & Scientific Affairs (m / w / d)

ADMHeidelberg
Praktikant Regulatory & Scientific Affairs (m / w / d).Im Bereich Regulatory Affairs & Food Law am Standort Heidelberg.Startzeitpunkt : nach Vereinbarung. Dauer : 6 Monate (freiwilliges oder Pflicht-Prakt...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Medical Scientific Liaison Manager (m / w / d)

Medical Scientific Liaison Manager (m / w / d)

Inizio EngageBaden-Württemberg, DE
Unser Kunde, ein europäisches Pharmazieunternehmen, gehört weltweit zu den führenden pharmazeutischen Unternehmen in der Erforschung und Entwicklung innovativer Medikamente für den therapeutischen ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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(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
Vor 30+ Tagen
Anstellungsart
  • Vollzeit
  • Homeoffice
Stellenbeschreibung

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 innovations for structural heart disease and critical care.

Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our T ranscatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient’s unmet clinical needs. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

Your key responsibility will be developing relationships with heart failure specialists and general cardiologists , as well as in the interventional community, to increase awareness of interventional strategies for treating atrioventricular valve regurgitation. Building referral practices in the field and driving alignment, adoption and execution of clinical trial therapy development initiatives, especially focused on assigned area, will be your core duties.

Candidate location : Germany. Some level of travelling will be requested - ca. 25 - 30 % (mainly inside Germany and EU congresses, society meetings) .

Apply in English!

How you will make an impact :

  • Identify restrictions to patient access within a region’s geography. Evaluate and identify creative sources and solutions that can help inform and influence the strategic business plan for patient outreach initiatives (e.g., recruitment events) for the mitral and tricuspid patient along the clinical trial continuum in collaboration with stakeholders (e.g., physicians, research coordinators). Establish an understanding of referral dynamics and how patient access may be restricted or delayed within the clinical trial pathway
  • Develop new and existing relationships with HCPs (e.g., physicians and key staff) through regular outreach and education activities, referring HCP visits, product demonstration and conference participation within the clinical research
  • Develop HCP- and patient-directed materials to support strategic business plan in collaboration with clinical marketing
  • Provide technical expertise on devices / protocols and on-site support for patient selection, screening, imaging, Heart Team concept and clinical data across BU (TMTT mitral and tricuspid therapies)
  • Define areas of opportunity along the Heart Team referral pathway to maximize their patient access to key clinical trials
  • Identify, influence and meet with existing HCPs to identify clinical needs and constraints related to BU clinical trial protocol adoption
  • Build timelines and key deliverables to align with overall business objective.
  • Provide technical guidance on a variety of projects including identifying trial site specific bottlenecks and work with clinical affairs to refer to cross-functional partners (e.g., training, trial management, screening etc.)
  • Identify and differentiate root cause of patient access restrictions between outreach and patient pathway ; Accurate tracking and documentation of all activity per clinical trial guidelines

What you'll need (Required) :

  • Bachelor's Degree or equivalent in or equivalent four (4) year clinical degree in Life Sciences or related field required - scientific / clinical background required
  • 10 years years experience required
  • Heart Failure experience from pharma or medical devise required, very beneficial
  • Experience as a Clinical Specialist, Therapy Development Specialist, Clinical Education and / or equivalent within the interventional cardiology industry preferred
  • Knowledge of clinical trials preferred
  • German and English fluent
  • What else we look for :

  • Proven successful project management skills
  • Proven expertise in both Microsoft Office Suite, including advanced Excel and related systems
  • Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
  • Recognized as an expert in own area with specialized depth and breadth of expertise
  • Extensive understanding of related aspects of therapy development
  • Strict attention to detail
  • Ability to interact professionally with all organizational levels
  • Ability to manage competing priorities in a fast paced environment
  • Ability to represent leadership on sections of projects within a specific area interfacing with project managers and cross-functional team(s)
  • Ability to consult in a project setting
  • Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence / control
  • What is it like to work at Edwards Lifesciences in Germany?

    As a global leader in patient-focused medical innovations, we offer rewarding opportunities and exciting challenges in a truly international, dynamic and friendly work environment.

    We are committed to fostering a diverse and inclusive work environment where all employees can grow, personally and professionally. To achieve this, we offer on-the-job development, training opportunities and the support and guidance provided by dedicated employee groups (the Edwards Network of Women, Edwards Foundation charity team, sustainability activities, and others).

    Edwards Lifesciences in Germany also offers the following benefits :

  • Competitive Compensation and Benefits package
  • Flexible working hours, remote working
  • Pension plan Risk
  • Insurance Meal Benefits
  • Service Awards Enhanced
  • Leave Benefits
  • Transportation Benefits
  • Employee Stock Purchase Programme
  • Employee Assistance Programme
  • Comprehensive Wellness Programme including onsite gym, yoga classes and massage, preventive health checks, healthy lifestyle webinars, educational events, charity activities and much more.
  • Benefits are regulated by an internal policy which contains the full details regarding the entitlement and conditions for the benefits. Benefits policy and components may vary by location.

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