Research assistant Jobs in Odenthal
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Research assistant • odenthal
Zuletzt aktualisiert: vor 1 Tag
We are seeking a dynamic and driven German-speaking Marketing & Sales Assistant to join our team in Barcelona.This role offers a relocation bonus to help you make a smooth transition.Included f...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Woran Du bei uns mitarbeitest : .Mitarbeit an Studien und Marktanalysen.Pflege von Inhalten im Internet und Intranet.Erstellen von PowerPoint-Präsentationen.
Administrative Unterstützung der Abteilung...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
We are a market research company seeking a passionate and dedicated individual to join our team as a Market Researcher for the Automotive / Sports cars.
In this role, you will be responsible for con...Mehr anzeigenZuletzt aktualisiert: vor 1 Tag
Carglass® Deutschland ist Spezialist für die Reparatur und den Neueinbau von Fahrzeugglas.In Deutschland beschäftigt Carglass® rund 2.
Mitarbeiterinnen und Mitarbeiter, davon sind über 1.Etwa 550 Mi...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
MEAMA ist ein aufstrebendes Startup im Bereich Lifestyle und Genussmittel mit Schwerpunkt auf Kaffee- und Teekapseln.Wir legen Wert auf natürliche Inhaltsstoffe und umweltfreundliche Verpackungen.U...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Administrative Assistant About ArangoDB Founded in Germany and now headquartered in San Francisco, ArangoDB is the most highly scalable, open-source, Graph Database with AI / ML capabilities availabl...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Clinical Research Associate II (Germany)
AllucentCologne, North Rhine-Westphalia, Germany At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need acro...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Student Assistant - Office Administration (m / f / d)
ISCC System GmbHKöln Student Assistant – Office Administration.Working Student, Part-time • Köln.At ISCC we are a close team of highly motivated, supportive and committed young professionals with a multitude of backgro...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
- Gesponsert
Clinical Research Coordinator - Munich, Germany
PharmiwebCologne, DE Hobson Prior is seeking a Clinical Research Coordinator for a part-time contract role in Munich.This position focuses on data entry, resolving queries, and updating important study files.An immedia...Mehr anzeigenZuletzt aktualisiert: vor 27 Tagen
German Speaking Jr Sales & Marketing Consultant in Barcelona w / Relocation Bonus
Cross Border TalentsCologne, GermanyQuick Apply
Senior Software Architect msg Research (m / w / d)
msg systemsKöln, DE Senior Software Architect msg Research (m / w / d).Etablieren Sie mit uns technologische und methodische Innovationen, meistern Sie mit uns den Wissenstransfer und unterstützen Sie mit uns spannende Pr...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Praktikum Recruiting / Research
Time 4 Change GmbHKöln Als kompetentes Personalmanagement-Unternehmen mit bundesweiten Kontakten beraten wir Sie gerne individuell und vertrauensvoll.
Dabei nehmen wir Ihre beruflichen Zukunftspläne genauso ernst wie Ihre...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Operations Research Consultant
OMPCologne, Germany As a Operations Research Consultant, you‘ll join the Delivery team as part of the Customer Solutions organization.The Delivery team delivers the solution and assists customers before, during, and b...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Administrative Assistant (f / m / x) Data Science of Bioimages Lab
Uniklinik KölnKöln, North Rhine-Westphalia Assistance to group members in their interactions with the University and University Hospital administration.Organization of social and scientific events of the group.
Coordination of our collaborat...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Working Student (f / m / d) - International Business Research -
Pisacane Information Services GmbHKöln We are a provider of business research services with over 30 years of experience in helping our renowned Clients to better understand key players, markets and trends in a broad range of industries ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Werkstudent Research
Bank für Sozialwirtschaft AktiengesellschaftKöln, DE15,00 € stündlich
- Gesponsert
Research Engineer (m / w / d)
infodasKöln, DE Die Stelle ist am Standort Köln oder Bonn zu besetzen.Du konzipierst und erstellst geeignete prototypische Anwendungen unter Laborbedingungen.
Du begleitest Forschungsprojek...Mehr anzeigenZuletzt aktualisiert: vor 14 Tagen
Market Research industry - Automotive / Sports cars - Köln
CXGCologne, NRW, DEQuick Apply
Experte CX-Research (m / w / d)
Carglass GER 1Köln , HauptverwaltungVollzeit
Marketing and Field Research Assistant
Centre People AppointmentsGermany - Dusseldorf / Cologne WORKING HOURS : 08 : 30 - 17 : 00 (Mon- Thu), 08 : 30-16 : 00 (Fri).LOCATION : Suburb of Dusseldorf, Germany (work from home is available after completion of training period – this may change depending on th...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Buying Assistant
SnipesCologne, DE SNIPES ist einer der weltweit führenden Sneaker- und Streetwear-Retailer mit über 750 Stores und fast 10.Mitarbeitenden in Europa und den USA.
Wir begeistern unsere Kunden mit einem breit gefächerte...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Assistant Producer
Electronic ArtsCologne, Germany Requisition Number : 184717Can this position be remote? : No.We are a global team of creators, storytellers, technologists, experience originators, innovators and so much more.We believe amazing games...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Shop-Assistant
Meama Köln GmbHCologne, North Rhine-Westphalia, GermanyQuick Apply
- Gesponsert
IT & Business Administrator
ZOE Institute for Future-fit EconomiesKöln, Germany In this role, your focus will be on supporting our day-to-day operations.This is an assistant-role within our internal framework, and we envision you to grow gradually into managing our IT systems,...Mehr anzeigenZuletzt aktualisiert: vor 10 Tagen
Working Student - Administrative Assistant - Cologne, Germany
ArangoDBCologne, DEQuick Apply
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Clinical Research Associate II (Germany)
AllucentCologne, North Rhine-Westphalia, GermanyVor 30+ Tagen
StellenbeschreibungGoverns quality standards for trial monitoring activities. Performs Selection, Initiation, Monitoring and Closure Visits at Investigator Sites according to project schedule. Adheres to project guidelines and Allucent SOPs for monitoring requirements. Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols. Tracks and supervises collection of ongoing study data for purpose of regular project status reporting. Collects and reviews regulatory documents as required. Prepares site visit reports and telephone contact reports. Maintains and updates CTMS in compliance with SOPs and study-specific directives. Acts as Document Owner for collected documents. May participate in the start-up process including preparing Informed Consent forms, developing study documents, EC / CA submissions, and / or site contract management Aims to pro-actively prevent and / or mitigate issues. Resolves site issues, including site recruitment challenges, and determines status for IP shipment. Acts as the main line of communication between the project team and the site staff. Works in collaboration with Allucent Centralized Monitoring Team to evaluate risk-based monitoring activities to facilitate oversight of the study conduct at the sites and prevent issues. Activities are related to but not limited to : Investigational Product supplies, non-IP study supplies, subject eligibility, protocol compliance, facilities, and PI oversight. Identifies potential logistical / practical problems and support Project team to create solutions / contingency plans, with timeframes for resolution. Ensures the continuous maintenance of the Trial Master File and Investigator Site File. Assists the Project Manager (PM) and Clinical Team Leader (CTL) with generation of study specific forms for completion by CRA and Investigators and follow up with the teams to ensure timely completion and submission. Works with Project Manager (PM); Clinical Team Leader (CTL), SSU (Study Start Up) team members or sponsor to ensure authorization of regulatory documents and site contracts. Attends Investigator Meetings (IM) to include organizing and presenting at investigator meetings. and study specific training meetings. May translate, coordinate translations or review completed translations of the essential documents as required. May participates in feasibility and / or site identification activities. Contacts local opinion leaders, medical consultants or specified investigators and identifies sites with the potential for participation. May follow feasibility procedures for documentation of feasibilities performed in collaboration with the Study Start Up Department. Where applicable, identifies the documentation required for review by Regulatory Authorities and Ethical Committees. May prepare Regulatory and Ethics Committee submissions working in conjunction with Study Start Up Department. Ensure written approvals are obtained and distributed appropriately prior to Site Initiation. Prepares and attends an Assessment Visit with a more senior CRA, CTL or Clinical Research Manager as required. May process interim and final payments to Investigators, including preliminary calculations, review and approval from Project Management, liaison with finance, logging trial expenditure, receipts, invoices, and income. Assists the Project Team with the day-to-day management of critical studies as required, including attendance at team meetings. Provides secondary in-house review of CRFs (if required). Support site staff in preparation for study related site audits and inspections. Where applicable, reports Quality Issues and supports the root cause analysis, writing of and resolution of the Corrective and Preventative Actions. May be assigned other tasks / activities / responsibilities related to the study execution in the country. May support initiatives in the country, GCO, and / or CTO to contribute to improvements and quality. Must work both independently and in a team environment. At least three years clinical monitoring experience and / or relevant clinical trial experience. Relevant life science degree / health care / nursing background and / or related degree. Sound knowledge of medical terminology and clinical monitoring process. Strong communication in Local and English language in both written and verbal skills. Strong interpersonal and organizational skills. Ability to translate guidelines, rules and regulations in clear and usable recommendations Representative, outgoing and client focused Ability to work in a fast-paced challenging environment of a growing company In-depth therapeutic and protocol knowledge Ability to travel for up to 8 days on site per month, depending on the project needs. In-depth therapeutic and protocol knowledge as provided in previous, or company provided training. Attention to detail. Ability to work independently and to effectively prioritize tasks, establish, and maintain strong working relationships with co-workers, managers, investigators, site personnel and clients. Demonstrated ability to manage multiple projects. Administrative excellence Proficiency with various computer applications such as Word, Excel, and PowerPoint required Demonstrated ability to develop, organize and manage new skills and tasks and mentor colleagues. Ability to manage multiple projects At least three years clinical monitoring experience and / or relevant clinical trial experience. Relevant life science degree / health care / nursing background and / or related degree. Sound knowledge of medical terminology and clinical monitoring process. Strong communication in Local and English language in both written and verbal skills. Strong interpersonal and organizational skills. Ability to translate guidelines, rules and regulations in clear and usable recommendations Representative, outgoing and client focused. Ability to work in a fast-paced challenging environment of a growing company. In-depth therapeutic and protocol knowledge. Ability to travel for up to 8 days on site per month, depending on the project needs. In-depth therapeutic and protocol knowledge as provided in previous, or company provided training. Attention to detail. Ability to work independently and to effectively prioritize tasks, establish, and maintain strong working relationships with co-workers, managers, investigators, site personnel and clients. Demonstrated ability to manage multiple projects. Administrative excellence. Proficiency with various computer applications such as Word, Excel, and PowerPoint required. Demonstrated ability to develop, organize and manage new skills and tasks and mentor colleagues. Ability to manage multiple projects. Comprehensive benefits package per location Competitive salaries per location Departmental Study / Training Budget for furthering professional development Flexible Working hours (within reason) Opportunity for remote / hybrid working depending on location Leadership and mentoring opportunities Participation in our Buddy Program as a new or existing employee Internal growth opportunities and career progression Financially rewarding internal employee referral program Access to online soft-skills and technical training via GoodHabitz and internal platforms Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our .
At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.
We are looking for a Clinical Research Associate II (CRAII) to join our A-team (hybrid
- remote). As a CRAII at Allucent, you will independently control and monitor investigation sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.
In this role your key tasks will include :
Requirements
To be successful you will possess :
To be successful you will possess :
Benefits
Benefits of working at Allucent include :
Disclaimers :
The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”
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