20 beste Stellen als quality coordinator in bayern – aktuell auf Personalsuche

Clinical Research Associate - Germany
Linical —München
- Hybrides Arbeiten
- Management-Erfahrung
- Englisch
- Forschungserfahrung
Marketing Coordinator (Content & Operations)
Jeavio —Bayern
- Vollzeit
- Marketing
- Projektmanagement
- Bachelor
Project Coordinator – HR Consultancy / Fluent English
atrain GmbH —Bamberg
- Vollzeit
- Projektmanagement
Workplace Supervisor
Autodesk —München
- Wochenendarbeit möglich
- Microsoft Word
- AutoCAD
- Microsoft Excel
Vice Principal City Campus part time 80% (m/f/d)
Bavarian International School gAG —München
- Teilzeit
- Forschungserfahrung
- Künstliche Intelligenz
- Führungserfahrung
Direkt bewerben
Senior Clinical Trial Coordinator
Alira Health —München
- Vollzeit
- Kundenberatung
- Forschungserfahrung
- Microsoft Office
BIM Coordinator (f/m/x)
Henn GmbH —München
- Abendschicht
- Tiefbau
City Campus PYP Coordinator - Primary Years Programme Coordinator (part-time 50%) (m/f/d)
Bavarian International School gAG —München
- Teilzeit
- Forschungserfahrung
- Führungserfahrung
- Unterrichten
Direkt bewerben
Senior Manager Group Audit Coordination & External Reporting (m/f/d)
INNIO —München
- Microsoft Excel
- Oracle
- Finanzwirtschaft
Direkt bewerben
Scientific Coordinator (m/f/d)
TUM Klinikum Rechts der Isar —München
- Teilzeit
- Doktorat
- Forschungserfahrung
- Mit Reiseanteil
6 Tage
Freelance In-Person Event Specialist - Munich, Germany
Visit.org —München
- Wochenendarbeit möglich
- Kundenberatung
Direkt bewerben
E2E Logistics & Safety Coordinator
Auterion —München
- Management-Erfahrung
- Bestandsmanagement
- ERP-Systeme
Direkt bewerben
14 Tage
Operations Manager
Gunnebo Entrance Control —München
- Vollzeit
- Hybrides Arbeiten
- Management-Erfahrung
- ERP-Systeme
- Projektmanagement
Direkt bewerben
Transformer Manufacturing Rules (TMR) Coordinator (m/f/d)
Siemens Energy —Nürnberg
- 60.785,90 € pro Jahr
- Vollzeit
- Produktion
Facility Coordinator
Cushman & Wakefield —München
- Vollzeit
Direkt bewerben
Business Applications & Automation Specialist (all genders) - Aerospace
Blackwave GmbH —Taufkirchen
- Vollzeit
- ERP-Systeme
- Datenanalyse
- Datenbanken
- Flexible Arbeitszeiten
Direkt bewerben
QM Coordinator
Dentsply Sirona —München
7 Tage
Chief of Staff
Hawk —München
- Vollzeit
- Finanzdienstleistungen
- Künstliche Intelligenz
Packaging Design & Execution Coordinator (m/f/d)
Maria Galland International GmbH —München
- Vollzeit
- Hybrides Arbeiten
- Microsoft Office
14 Tage
HR COORDINATOR GAS (m/w/d)
NBCUniversal —München
- Vollzeit
- Hybrides Arbeiten
- Microsoft Powerpoint
- Microsoft Excel
- Kundenberatung
14 Tage

Ich möchte aktuelle Job-E-Mails für Stellen als quality coordinator in bayern erhalten

Wenn Sie sich bei Ihrem Konto anmelden, stimmen Sie den Nutzungsbedingungen, den Richtlinien zur Verwendung von Cookies sowie der Datenschutzerklärung von SimplyHired zu.

Weitere Job-Standorte erkunden

quality coordinator jobs near bayern

Jobs als Clinical Trial Manager in München

Jobs als Mergers Acquisitions Manager in München

Jobs als Operations Manager in München

Jobs als Clinical Research Associate in München

Jobs als Chief Of Staff in München

Jobs als Logistics Coordinator in München

Jobs als Senior Auditor in München

Jobs als Campus Manager in München

Jobs als Packaging Designer in München

Jobs als Manager Of Workplace Operations in Berlin

Jobs als People Operations in Berlin

Jobs als People & Culture Manager in Stuttgart

Jobs als Marketing Coordinator in Frankfurt Am Main

Jobs als Marketing, Öffentlichkeitsarbeit in Magdeburg

Jobs als Junior Marketing Manager in Frankfurt Am Main

Jobs als Marketing Coordinator in Düsseldorf

Jobs als Marketing Coordinator in Berlin

Jobs als Marketing Remote in Hamburg

Jobs als Hr Consultant in Stuttgart

Jobs als Hr in Augsburg

Clinical Research Associate - Germany

Linical -
München

Jetzt bewerben

Details zur Stelle

Qualifikationen

Management-Erfahrung
Englisch
Forschungserfahrung
Deutsch
Zeitmanagement

Vollständige Stellenbeschreibung

The Clinical Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites.

Major responsibilities include ensuring the safety and well-being of study participants at assigned sites, ensuring site compliance with Good Clinical Practice (GCPs), applicable regulations, the protocol and study plans; ensuring data integrity through source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements.

EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while the Clinical Operations Manager (COM) will oversee the CRA role.

Duties and Responsibilities

Participates in the identification of potential investigative sites, conducts site qualification visits, collects, and reviews site regulatory documents, and prepares site qualification visit reports and associated documentation; participates in the final selection of investigative sites
Conducts site initiation visits; trains site personnel on Client and regulatory requirements for study conduct; participates in and/or conducts site meetings and investigator meetings, and prepares site initiation visit reports and associated documentation
Conducts site monitoring visits and follow-up to identify significant problems and issues, and to ensure that all clinical aspects of studies are being carried out in accordance with study plans, GCPs, and applicable regulations; prepares monitoring visit reports and associated documentation
Reviews on-site files and records, Case Report Forms, and source documents for completeness, accuracy, consistency, and compliance; identifies deficiencies and discrepancies; initiates corrective action as required
Assists in submissions to the Independent Ethics Committees (central and local) and to Competent / Regulatory Authorities
Arranges site payments and facilitates site budgets and contracts as requested
Ensures training is performed within a reasonable period and is current and appropriately documented
Ensure protocol deviations are appropriately documented, and action items are followed through to completion
Manages site monitoring visit schedule, and the follow-up of issues between visits, along with ongoing regular communication with the sites and the clinical study team
Maintains close contact with the site staff, to be aware of patient enrolment, enrolled patients’ status, IP supply and any further site requests or issues
Ensures essential documents are filed in the Trial Master File (TMF) according to the project guidelines
Ensures appropriate and timely transmission of clinical data to data management; reviews data queries, and clarifies and/or obtains changes to data as appropriate
Conducts site close-out visits to include final IP reconciliation and disposition, review of completeness and accuracy of files, and retrieval of documents for the TMF; prepares site close-out visit reports and associated documentation
Attend team meetings as required
Participates in systems User Acceptance Testing as required
Senior CRA assists with the development and implementation of study-specific monitoring and reporting procedures, methods, guidelines, and tools; participates in development of participant tracking systems; conducts monitoring assessment visits for the purpose of rescuing a troubled site or performing audit preparation at the direction of the CTM
Senior CRA oversees work for assigned CRAs on a designated project; reviews and approves monitoring visit reports; manages the visit schedule; provides feedback during the annual review process regarding performance of assigned CRAs
Other duties as assigned

Required Skills and Abilities

Require a minimum of four years’ clinical research experience (e.g., Clinical Trial Associate, Study Coordinator) or equivalent.
Life Science degree or equivalent experience combined with successful completion of a recognized CRA training program is essential
Requires a minimum of two years’ monitoring and site management experience as Clinical Research Associate
Pulmonology and Oncology therapeutic expertise
Excellent understanding of the clinical research process, clinical trial-related systems and procedures, regulations and GCPs, and the scientific/clinical knowledge to be able to understand the nature of drugs being studied
Excellent written and verbal communication skills, and time management, organizational and problem-solving skills
Fluent in German language (speaking, writing) and good comprehension of English language where English is not the local language
Excellent people skills and ability to work successfully in a matrixed team environment
Dedication to quality in all work tasks and deliverables
Ability to prioritize and manage multiple tasks as necessary, including during travel and monitoring visits
Working knowledge of computer systems, applications, and operating systems
Ability to travel up to 75%
Possess a valid driver’s license, as required

Jetzt bewerben

Erweiterte Suche

quality coordinator Jobs in bayern

Clinical Research Associate - Germany

Marketing Coordinator (Content & Operations)

Project Coordinator – HR Consultancy / Fluent English

Workplace Supervisor

Vice Principal City Campus part time 80% (m/f/d)

Senior Clinical Trial Coordinator

BIM Coordinator (f/m/x)

City Campus PYP Coordinator - Primary Years Programme Coordinator (part-time 50%) (m/f/d)

Senior Manager Group Audit Coordination & External Reporting (m/f/d)

Scientific Coordinator (m/f/d)

Freelance In-Person Event Specialist - Munich, Germany

E2E Logistics & Safety Coordinator

Operations Manager

Transformer Manufacturing Rules (TMR) Coordinator (m/f/d)

Facility Coordinator

Business Applications & Automation Specialist (all genders) - Aerospace

QM Coordinator

Chief of Staff

Packaging Design & Execution Coordinator (m/f/d)

HR COORDINATOR GAS (m/w/d)

Ich möchte aktuelle Job-E-Mails für Stellen als quality coordinator in bayern erhalten

Weitere Job-Standorte erkunden

Tools für Jobsuchende

Arbeitgebertools

Durchsuchen

Bleiben Sie in Kontakt