Clinical Site Monitor I/ II - FSP/ Germany/Homebased
Home Office
Vollzeit
Parexel
… FSP is hiring for a home-based Clinical Site Monitor I or II. Single sponsor dedicated to a worldwide biopharmaceutical company that relentlessly seeks … Parexel FSP is hiring for a home-based Clinical Site Monitor I or II. Single sponsor dedicated to a worldwide … level. Experience required: A minimum of 1 year experience as a Clinical Research Associate with demonstrated experience in monitoring (virtual or onsite). …Research Associate SponsorBusiness Development Manager
München
Vollzeit
Alira Health
… new people. Previous experience using a CRM system preferred We will not sponsor applicants for work visas. Languages German Education Bachelor of Science … The BD Manager is an important member of the Alira Health Research and Clinical Development (RCD) team. The Manager will be responsible for facilitation … Manager ROLE The BD Manager is an important member of the Alira Health Research and Clinical Development (RCD) team. The Manager will be responsible for …Associate Sponsor Dedicated StellenangeboteTrial Coordinator (Germany)
Deutschland
Vollzeit
Lindus Health
… Working with the Lindus Health clinical team to respond to queries from Sponsor or regulatory authorities Contributing to our clinical strategy as an … Our mission All new medicines need to undergo clinical trials to show they’re safe and effective. But today’s clinical trial … literacy Able to adapt and learn to use new technology to change the way research is delivered Experience and understanding of research and clinical trials …Clinical Research Dedicated Stellenangebote
Finance Study Start-up Manager / Sponsor-dedicated / Based in Munich, Germany
München
Home Office
Fortrea
… organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, … As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of …Clinical ResearchClinical Data Manager (remote, full-time)
Home Office
Vollzeit
P95
… will have 3 – 5 years of DM experience with a minimum of 1 year’s direct sponsor management. Knowledge of the clinical trial process, Data Management, … Report, Data Cleaning Plan... Send the Data Clarification Forms/queries to clinical sites and ensure that clinical data has been updated Define and perform … Why us? You will join a young, very dynamic, and fast-growing private research organization. Our passionate, truly multicultural, and diverse team of …Clinical Research AssociateClinical Associate
Frankfurt am Main
Vollzeit
Icon plc
… of slides, overheads, etc., as needed for project, departmental, sponsor and/or business development presentations. To assist with the coordination … About the role ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical … the role ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research …Clinical Research AssociateProjektmanagerin (w/m/d) für klinische Studien
Kiel
Vollzeit/Teilzeit/Ausbildung
KKS Netzwerk
… Koordinierung von Schnittstellen in interdisziplinären Teams (Sponsor, Prüfer, Biometrie, Datenmanagement, Monitoring etc.) … für Ärzte und Studienpersonal Das bringen Sie mit: Hochschulstudium Clinical Trial Management, der Naturwissenschaften oder vergleichbare Ausbildung …Clinical Research Associate Sponsor Stellenangebote
Clinical Operations Lead
Home Office
Vollzeit
Alimentiv
… team, as well as individual/country CRA calls Attend meetings with Study Sponsor to provide status updates on country and site progress Provide operational … Responsible for the clinical operations of a project within a defined regional/global level. Provides … level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring …Associate Sponsor
Clinical Research Associate, sponsor dedicated
Home Office
Vollzeit
ICON
The Clinical Research Associate will perform site activities for Phase I-IV studies … The Clinical Research Associate will perform site activities for Phase I-IV studies operating as … The Clinical Research Associate will perform site activities for Phase I-IV studies operating as the main …Clinical Research Sponsor Dedicated StellenangeboteClinical Research Associate (all levels), Oncology, FSP, home based, client dedicated
Home Office
Vollzeit
Syneos - Clinical and Corporate - Prod
Description Clinical Research Associate - home based, sponsor dedicated, flexible level based on your work experience Come discover what … Description Clinical Research Associate - home based, sponsor dedicated, flexible level based … Description Clinical Research Associate - home based, sponsor dedicated, flexible level based on your …Research DedicatedClinical Research Coordinator I
Hamburg
Vollzeit
Velocity Clinical Research, Inc.
… queries Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information Ensure … Overview: Velocity Clinical Research is an owned and integrated research site organization, providing … Overview: Velocity Clinical Research is an owned and integrated Research site organization, providing …Clinical Associate Sponsor StellenangeboteGlobal Clinical Quality Assurance Manager (m/f/d)
Hamburg
Vollzeit
Olympus Europa SE & Co. KG (OEKG)
… interacting with FDA and/or other health authority inspections of sponsor, investigator site(s), and/or CRO(s). Ability to represent the company in … with applicable regulations and industry best practices, participate in clinical process improvement projects and initiatives for development, enhancement … vendors where applicable Experience auditing clinical vendors, Clinical Research Organizations (CRO) and internal clinical programs Experience leading, …Research Sponsor StellenangeboteStudienassistenz/Study Nurse (m/w/d) Abteilung Molekulares Neuroimaging
Mannheim
Vollzeit/Teilzeit/Ausbildung
Zentralinstitut für Seelische Gesundheit
… Initiierungen und Monitoring Visits Ansprechpartner und Schnittstelle für Sponsor, Monitor, Prüfgruppe und Patient Pflege des ISF und Pflege des TMF bei … Für die Durchführung früher klinischer Studien steht eine moderne Early Clinical Trials Unit (ECTU), eine Forschungsstation mit sechs Betten, zur …Research Sponsor Dedicated Stellenangebote
Study Start Up Associate I
Home Office
Vollzeit
ICON
… and all applicable regulations, laws, ethical standards, other guidelines, sponsor requirements Ensure that the overall process is focused on quality, … ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment … ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving …Clinical Stellenangebote