20 beste Stellen als regulatory project in bayern – aktuell auf Personalsuche

Study Start Up Associate
Alira Health —München
- Vollzeit
- Microsoft Office
- Bachelor
Senior Regulatory and Start-up Specialist - Germany
Optimapharm d.o.o. —München
- 65.000 € – 70.000 € pro Jahr
- Vollzeit
- Homeoffice
- Forschungserfahrung
- Microsoft Office
- Master
- Flexible Arbeitszeiten
- Empfehlungsprogramm
14 Tage
Regulatory Consultant
Yordas Group —Forchheim
- Vollzeit
- Homeoffice
- Englisch
- Kommunikationsfähigkeit
Direkt bewerben
8 Tage
Clinical Trial Manager / Local Study Manager
サイネオス・ヘルス —München
- Forschungserfahrung
- Projektmanagement
- Bachelor
Clinical Trial Manager
Ambu —Augsburg
- Vollzeit
- Hybrides Arbeiten
12 Tage
Consultant Sustainability (m/f/d)* in full- or part time (80%) - limited until 06/2027
Munich Re —München
- Teilzeit
- Hybrides Arbeiten
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Office
9 Tage
Site Activation Specialist - Germany
IQVIA —München
- Vollzeit
- Bachelor
12 Tage
Project Quality Manager (m/f/d)
Fluence Energy —Erlangen
- Vollzeit
- Microsoft Office
- Master
- Bachelor
9 Tage
Project Manager Global Quality (f/m/d)
Aenova Holding —Starnberg
- Vollzeit
- Projektmanagement
- Mit Reiseanteil
- Kommunikationsfähigkeit
Project Manager, IVV, Satellite Systems, IRIS2 Programme Office
SES —München
- PMP
- Englisch
- Master
CRA II Germany - eastern Germany (Leipzig, Halle, Berlin)
サイネオス・ヘルス —München
- Bachelor
- PC-Kenntnisse
Clinical Operations Specialist with focus on finance
サイネオス・ヘルス —München
Manager, Pharmacovigilance Quality Assurance
Novartis —München
- Vollzeit
- Wartung
- Englisch
Manager Quality & Regulatory Affairs for AI Medical Software - (w/d/m)
deepeye Medical GmbH —München
- Hybrides Arbeiten
- Master
- Künstliche Intelligenz
- Flexible Arbeitszeiten
Direkt bewerben
Senior Clinical Trial Coordinator
Alira Health —München
- Vollzeit
- Kundenberatung
- Forschungserfahrung
- Microsoft Office
Associate Sustainability Specialist (f/m/x)
Tanso Technologies GmbH —München
- Vollzeit
- Hybrides Arbeiten
- Künstliche Intelligenz
Senior Specialist (m/f/d) – Quality Assurance / Regulatory Affairs – temporary December 2027
Vantive —München
- Textverarbeitung
- ERP-Systeme
- Projektmanagement
Intern - Allianz Services - Compliance and Regulatory (m/f/d)
Allianz —München
- Teilzeit
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Office
- Flexible Arbeitszeiten
Sustainability Manager (f/m/d)
Siemens —Erlangen
- Vollzeit
- Master
Project Leader, Risk & Compliance – Market & Commodity Risk (Energy Trading)
Boston Consulting Group —München
- Vollzeit
- Künstliche Intelligenz
- Führungserfahrung
- Analytik
9 Tage

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Study Start Up Associate

Alira Health -
München

Jetzt bewerben

Details zur Stelle

Vollzeit

Qualifikationen

Microsoft Office
Bachelor
Klinische Studien

Vollständige Stellenbeschreibung

Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you.

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

The Study Start Up (SSU) Associate function is to support the SSU Manager with all SSU-related activities in collaboration with other clinical research stakeholders and to serve as a contact for local/global SSU process improvements.

Job Description

THE STUDY START UP ASSOCIATE ROLE

KEY RESPONSABILITIES

Coordinates and assists with all start up activities prior to site activation, including but not limited to:

Submission of required documents to ethic committees, regulatory authorities, sites and sponsor.
Submission of the clinical study agreement for review, as needed.
Contribution to/coordination of site Informed Consent Form (ICF) localization and guidance in line with regulatory / health authority requirements.
Contribution to localize global Informed Consent Form (ICF) with country requirements.
Understanding and dissemination of information related to Ethics Committee, meeting dates & costs to relevant stakeholders.
Understanding and dissemination of information related to Ethics applications & associated online systems.
Clinical Trial Health Authority application and regulatory submission process.
Supporting with the Contracts & Indemnity request process.
Collation/provision of other materials and documentation used by the study requiring local governance approval.
Maintain up to date knowledge, ensuring study adherence and compliance with local regulatory requirements and associated documentation in line with SSU Manager oversight/input.
Contribute to collation of metrics to ensure processes are in place that drive efficiency and reduction of timelines across start up and contract negotiation.
Ensure all start up information & requirements are kept up to date in a central repository for project teams.
Track metrics and study start-up timelines to identify trends and opportunities for improvement.
Provide continuous and proactive communication with ECs / hospital administration / industry bodies to obtain accurate and up to date information on clinical trial status and activities.
Assist with identification and tracking of new sites in collaboration with CRAs.

DESIRED QUALIFICATION & EXPERIENCE

University Degree or equivalent preferably in a medical/science-related field.
Prior work experience demonstrating knowledge and understanding of clinical trials.
Demonstrated knowledge and understanding of ICH-GCP and a desire to increase specialist knowledge in regulatory, ethics and contractual requirements for SSU in clinical trials for European and international trials.

TECHNICAL COMPETENCES & SOFT SKILLS

Good communications skills including the ability to: ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution.
Ability to present clear messages from complex information/data to all levels in the organization in both written and spoken English.
Experience in working as part of a team with a proven ability to make an active contribution to the team's performance and teamwork.
Self-motivated, assertive, and displays initiative.
Proven organizational skills and the ability to prioritize and manage multiple tasks with flexibility.
Demonstrated computer literacy, usage of MS Office software, web-based systems and databases.
Availability to travel domestically and internationally if required.

WORKING CONDITIONS/PHYSICAL DEMANDS

Normal office working conditions including frequent sitting, standing, bending, twisting and computer monitor use. Occasional lifting of weight up to 30 lbs.

Languages

English

Education

Bachelor of Science (BS): Life Sciences, Bachelor of Science (BS): Medicine

Contract Type

Regular

Jetzt bewerben

Erweiterte Suche

regulatory project Jobs in bayern

Study Start Up Associate

Senior Regulatory and Start-up Specialist - Germany

Regulatory Consultant

Clinical Trial Manager / Local Study Manager

Clinical Trial Manager

Consultant Sustainability (m/f/d)* in full- or part time (80%) - limited until 06/2027

Site Activation Specialist - Germany

Project Quality Manager (m/f/d)

Project Manager Global Quality (f/m/d)

Project Manager, IVV, Satellite Systems, IRIS2 Programme Office

CRA II Germany - eastern Germany (Leipzig, Halle, Berlin)

Clinical Operations Specialist with focus on finance

Manager, Pharmacovigilance Quality Assurance

Manager Quality & Regulatory Affairs for AI Medical Software - (w/d/m)

Senior Clinical Trial Coordinator

Associate Sustainability Specialist (f/m/x)

Senior Specialist (m/f/d) – Quality Assurance / Regulatory Affairs – temporary December 2027

Intern - Allianz Services - Compliance and Regulatory (m/f/d)

Sustainability Manager (f/m/d)

Project Leader, Risk & Compliance – Market & Commodity Risk (Energy Trading)

Ich möchte aktuelle Job-E-Mails für Stellen als regulatory project in bayern erhalten

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THE STUDY START UP ASSOCIATE ROLE

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DESIRED QUALIFICATION & EXPERIENCE

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