20 beste Stellen als clinical data in berlin, be – aktuell auf Personalsuche

Clinical Research Coordinator
Parexel —Berlin
- Wochenendarbeit möglich
- Windows
- PC-Kenntnisse
Clinical Research Associate / Klinischer Monitor (m/w/d)
IGES GmbH —Berlin
- Online-Bewerbung
- Englisch
- Analysefähigkeit
- Organisationstalent
- Homeoffice-Möglichkeit
- Flexible Arbeitszeiten
Direkt bewerben
Clinical Trial Manager (f/m/d)
Nia Health GmbH —Berlin-Kreuzberg
- Teilzeit
- Medizin
- Doktorat
- Krankenhaus
- Weiterbildungsprogramme
Direkt bewerben
Clinical Research Associate II/III - Germany
Optimapharm d.o.o. —Berlin
- 50.000 € – 60.000 € pro Jahr
- Vollzeit
- Homeoffice
- Nursing
- Forschungserfahrung
- Master
- Flexible Arbeitszeiten
- Empfehlungsprogramm
Talent wanted (all)
mediaire GmbH —Berlin
- Vollzeit
Direkt bewerben
Mental Health Expert, Part-Time (German Speaking)
mpathic —Berlin
- 30 € – 50 € pro Stunde
- Teilzeit
- Homeoffice
- Microsoft Office
- Master
- Psychologie
Direkt bewerben
Senior Clinical Research Associate
Veranex, Inc. —Berlin
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Direkt bewerben
11 Tage
Position: Clinical Operations Manager
Meditrial Europe Ltd. —Berlin
- Vollzeit
- Englisch
- Forschungserfahrung
- Master
Medical Science Liaison – Neurology (Migraine)
Organon —Berlin
- Vollzeit
- Doktorat
- Projektmanagement
Direkt bewerben
Quality Control Assistant [Temporary Contract]
Parexel —Berlin
- Englisch
- Windows
- PC-Kenntnisse
Medical Writer (w/m/d)
Flinn.ai —Berlin
- Vollzeit
- Hybrides Arbeiten
- Doktorat
- Vertrieb
- Bachelor
- Flexible Arbeitszeiten
Direkt bewerben
Clinical Operations & Enablement Lead
Nucs AI —Berlin
- Vollzeit
- Hybrides Arbeiten
- Schreibfähigkeiten
- Forschungserfahrung
- Master
Direkt bewerben
Bachelor's & Master's Thesis Opportunities - AI, Medical Imaging & Clinical Software
Nucs AI —Berlin
- Vollzeit
- Hybrides Arbeiten
- Informatik
- Master
- Bachelor
Direkt bewerben
MSL Germany
Curium Pharma —Berlin
- Master
Technical Co-Founder & CTO (PreSeed Health-tech) Hospital Discharge Readiness Engine
Founders Factory —Berlin
- Vollzeit
- Hybrides Arbeiten
- Krankenhaus
- Systemdesign
- APIs
Direkt bewerben
4 Tage
Physician Annotator - Nuclear Medicine Clinical AI (Part-Time/Contract)
Nucs AI —Berlin
- Vollzeit
- Homeoffice
- Künstliche Intelligenz
- Flexible Arbeitszeiten
Direkt bewerben
Co-Found with Founders Factory - Healthcare Studio
Founders Factory —Berlin
- Hybrides Arbeiten
Direkt bewerben
Clinical Practice Support Expert, Removables (Germany)
Dandy —Berlin
- 49.500 € – 55.000 € pro Jahr
- Vollzeit
- Hybrides Arbeiten
- CAD
- Kommunikationsfähigkeit
Data Engineer (Databricks)
wega Informatik —Berlin
- Vollzeit
- Informatik
- AWS
- Machine Learning
Clinical Trials Business Development Representative
Milestone One —Berlin
- Vollzeit
- Homeoffice
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Direkt bewerben

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Clinical Research Coordinator

Parexel -
Berlin

Jetzt bewerben

Details zur Stelle

Qualifikationen

Windows
PC-Kenntnisse

Vollständige Stellenbeschreibung

The Clinical Research Coordinator is accountable for the planning, preparation, and execution of clinical trials in conjunction with the Team Leader, Project Manager, and Investigator. This role ensures that clinical studies are conducted according to the study protocol, ICH GCP guidelines, and unit SOPs. The coordinator assists in the conduct of Phase I-III studies across all therapeutic areas, ensuring studies are prepared to the highest standard within specified timelines. The role also involves clinical conduct oversight, data cleaning, and deviations management.

Key Accountabilities:

Technical supervision of Clinical Research Nurse, assigned to the studies
Control and direct activities and staff during key operational aspects of assigned studies
Organization and Preparation of clinical studies, as listed below:
- Study Protocol review and study feasibility prove
- Review of all other study related documents e.g., CRF, Lab Manual, Reference Manual
- Review Protocol Deviation Assessment Plan (PDAP) and Data Verification Specification (DVS). Be involved in project development, taking part in early internal project discussions.
- Early recognition of areas of potential problems, provide contingency plans or address the issue in an appropriate way with the required departments and give input into possible solutions (RACT).
- Escalate issues as soon as possible. Open QI in timely manner, close actions on or before the end date.
- Record Clinical including medical deviations on the Observable protocol deviations (PD) log.
- Review combined PD log.
- Generation of general working instructions, source data sheets and other relevant forms and documents for the allocated clinical studies
- Generation and maintenance of the general and emergency case files, Staff Log, Window Allowance Agreement, Source Data Verification
- Training / Training organization of personnel assigned to the study
- Organization of study specific training
- Organization of the generation of dietary plans/meal plans
- Verification and maintenance of the file containing the volunteers informed consent forms
- Organization of study specific material and medical devices
- Lead ClinBase setup development across pharmaceutical services, laboratory, database design, and clinical operations for all assigned studies
- Monitor that ClinBase set up activities and ensure that it is developed within the given time.
- Prepare ClinBase set-up requirements forms for Screening and Experimental.
- If EDC is in use review annotated CRF and perform UAT.
- Review the ClinBase set up procure list, time windows, normal ranges as part of pre-dummy review.
- Check User Defined Procedures on Feasibility
- Approve the set up for Clinical use to ensure study requirements are captured as per protocol and in accordance with sponsor requirements (WAA, Normal Ranges, Lab Profile, order of procedures, relative time User Defined Procedures)
- Initiate ClinBase revisions and subsequent approval.
- Care support of the volunteers participating in a study from admission to discharge
- Coordination of study-preparations on the ward incl. providing medical technique, sample container, documentation computers, bed
- Providing study relevant shift to shift information
- Ensuring all study related assessments and medical measurements will be performed according to study protocol and relevant clinical guidelines (GCP and ICH guidelines)
- Ensuring all study relevant documentations are going to performed according to study protocol and ICH/GCP guidelines
- Overseeing, maintaining, and leading the processes and progresses of all allocated studies in conjunction with study physician, project management and data management
- Volunteer payment management
- Management/Organization of medication storage, drug check in and out
- Issuing of Audit Reports on internal and external quality audit findings
- Resolution of data clarification queries
- Management of CRF Shipment, Source Data storing and archiving after study finalization

Cooperation with the study monitor, incl. preparation for monitor visits, cleaning and correcting of study relevant documents according to monitor/protocol demands
Perform investigations on subjects (physiological measurements including ECG, Blood Pressure, Lung Function, venous puncture and other) according to the study protocol
Use of psychological and physiologic test procedures
Cooperation with other internal departments as a company’s study team member
Participation in project team meetings
Study presentation in internal study initiation meetings
Participation in client meetings
Administration of Investigational Products
Other tasks in the opinion of the manager and need of the CPRU.

Skills:

Fluent knowledge of German and Intermediate English skills (written and spoken)
Computer skills (Windows Office)
Organizational talent
Ability to work under pressure and flexibility in working times (early, late and night shifts)
Ability to work on weekends and holidays
Knowledge of ICH-GCP Guidelines.

Knowledge and Experience:

Relevant experience in hospitals or medical surgery.

Education:

Terminated education as nurse, MTA, doctor´s assistant, paramedic, or similar/equivalent qualification/education.

Jetzt bewerben

Erweiterte Suche

clinical data Jobs in berlin, be

Clinical Research Coordinator

Clinical Research Associate / Klinischer Monitor (m/w/d)

Clinical Trial Manager (f/m/d)

Clinical Research Associate II/III - Germany

Talent wanted (all)

Mental Health Expert, Part-Time (German Speaking)

Senior Clinical Research Associate

Position: Clinical Operations Manager

Medical Science Liaison – Neurology (Migraine)

Quality Control Assistant [Temporary Contract]

Medical Writer (w/m/d)

Clinical Operations & Enablement Lead

Bachelor's & Master's Thesis Opportunities - AI, Medical Imaging & Clinical Software

MSL Germany

Technical Co-Founder & CTO (PreSeed Health-tech) Hospital Discharge Readiness Engine

Physician Annotator - Nuclear Medicine Clinical AI (Part-Time/Contract)

Co-Found with Founders Factory - Healthcare Studio

Clinical Practice Support Expert, Removables (Germany)

Data Engineer (Databricks)

Clinical Trials Business Development Representative

Ich möchte aktuelle Job-E-Mails für Stellen als clinical data in berlin, be erhalten

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