Clinical affairs manager Jobs in Gräfelfing

Aufgaben Erstellung und Pflege der Country Knowledge Trackers Support der Project Managers Country Operations in. Site Management, Contract Negotiation, Study start up and follow up Management..

Clinical Evaluation Plan and Report, clinical content for regulatory submissions), including continuous.. subject matter expert adaptation and improvement of Clinical Affairs processes.Your profileEducation..

As a a Clinical Trial Manager you will be joining the world's largest & most comprehensive clinical.. As the Clinical Trial Manager you will working sponsor dedicated and will be responsible for the..

Join our diverse teams of passionate people and a career that allows you to develop both personally and professio nally. At Getinge we exist to make life saving technology accessib..

We are currently looking for a self driven and open minded Clinical Application Manager to join one of.. Also, daily cooperation with our clients is key. Clinical Application Manager (m f d) Tasks..

Unser Ziel. Opioide (Markt. 20 Mrd. Euro p.a.) zu ersetzen und chronischen Schmerzpatienten ein neues Leben zu schenken. Als Projektleiter. Project Manager (w m d) Clinical Trials verantwortest..

We are currently looking for a self driven and open minded Clinical Application Manager to join one of.. Also, daily cooperation with our clients is key. Tasks & Responsibilities. Be the Clinical Application..

Als Director des (clinical) QA RA Teams wirst Du in entscheidender Funktion hands on beteiligt sein an.. dabei stellst Du die Einhaltung von Good Clinical Practice (GCP) Vorgaben bei uns, unseren Vendoren und..

In der verantwortungsvollen Funktion als Manager Regulatory Affairs. (w m d) betreuen Sie eigenständig.. Ihre Bewerbung Haben wir Ihr Interesse für die Position Manager Regulatory Affairs (w m d) in München..

Overview Medpace is a full service clinical contract research organization (CRO). We provide Phase I IV clinical development services to the biotechnology, pharmaceutical and medical device..

Chargenprotokolle, Leistungsberichte, Zulassungsanträgen, Herstell. und Verpackungsvorschriften Erstellung und Review von SOPs Überwachung der GxP Compliance der Clinical Supply Chain..

All with the commitment and consent of the patient. Myoncare collects clinical patient data thanks to.. first hands as our new Quality and Regulatory Affairs Manager. Healthcare Technology (f m d..

Ihr Profil. Abgeschlossenes Studium im Bereich eHealth IT, Medizinische Dokumentation Informatik, Gesundheitsinformatik, Informationsmanagement im Gesundheitswesen, Data Science i..

Regulatory Procedural Management and Clinical Trial Lead (m f x), Regulatory Affairs Europe The Position.. In this role, lead EU & AMELA Regulatory Procedural Management and Clinical Trial Office providing..

internationally.About the roleThis Project Manager role will be an active team member.. You will be responsible for Planning and execution of clinical studies at national international..

Werde Teil der DENK Family und erlebe die Vielfalt unseres hochmotivierten Teams. Unsere Core Values, "WINNING MINDSET". "GET STUFF DONE". "HIGH FIVE". "WALK THE TALK" und..