19 beste Stellen als associate clinical trial in münchen – aktuell auf Personalsuche

Study Start Up Associate
Alira Health —München
- Vollzeit
- Microsoft Office
- Bachelor
Clinical Development Associate (m/f/d)
VeonGen Therapeutics GmbH —Planegg
- Forschungserfahrung
- Mit Reiseanteil
Clinical Research Associate
Alexion Pharmaceuticals,Inc. —München
- Bachelor
- Mit Reiseanteil
- Kommunikationsfähigkeit
Clinical Research Associate - Germany
Linical —München
- Hybrides Arbeiten
- Management-Erfahrung
- Englisch
- Forschungserfahrung
Clinical Research Associate I - Real World Late Phase
サイネオス・ヘルス —München
- Bachelor
- Wirtschaft
Clinical Research Associate based in Germany
Fortrea —München
- Vollzeit
- Nursing
- Management-Erfahrung
- Mit Reiseanteil
Clinical Trial Manager
サイネオス・ヘルス —München
- Bachelor
- Wirtschaft
5 Tage
Senior Clinical Research Associate
Veranex, Inc. —München
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Direkt bewerben
Clinical Research Associate / Senior Clinical Research Associate
PSI CRO —München
- Vollzeit
- Hybrides Arbeiten
- Englisch
- Microsoft Office
- Mit Reiseanteil
Direkt bewerben
CRA II/Sr CRA Germany - eastern Germany (Leipzig, Halle, Berlin)
サイネオス・ヘルス —München
- Bachelor
- PC-Kenntnisse
CRA II/Sr CRA based in Berlin or Hamburg
サイネオス・ヘルス —München
- Bachelor
Senior CRA - Phase I oncology trials - Hamburg/Berlin region
サイネオス・ヘルス —München
- Bachelor
Associate Director (m/f/d), Computational Pathology Biomarker Lead (Oncology/BioPharma)
AstraZeneca —München
- Doktorat
- Künstliche Intelligenz
- Python
- Aufstiegsmöglichkeiten
Country Study Manager
Alexion Pharmaceuticals,Inc. —München
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Office
(Senior) Scientist (f/m/d) - Immunomonitoring
Bavarian Nordic —Martinsried
- Vollzeit
- Doktorat
- Organisationstalent
Manager FSP 360
サイネオス・ヘルス —München
- Management-Erfahrung
- Bachelor
Senior CRA
Alira Health —München
- Vollzeit
- Management-Erfahrung
- Kundenberatung
- Forschungserfahrung
Senior CRA II Sponsor Dedicated based in Düsseldorf region
Fortrea —München
- Vollzeit
- Forschungserfahrung
- Bachelor
- Ohne Hochschulabschluss
Global Senior Project Specialist (Sponsor Dedicated) Germany
サイネオス・ヘルス —München
- Englisch
- Microsoft Office
- Mit Reiseanteil

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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

associate clinical trial Jobs in münchen

Study Start Up Associate

Clinical Development Associate (m/f/d)

Clinical Research Associate

Clinical Research Associate - Germany

Clinical Research Associate I - Real World Late Phase

Clinical Research Associate based in Germany

Clinical Trial Manager

Senior Clinical Research Associate

Clinical Research Associate / Senior Clinical Research Associate

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

CRA II/Sr CRA based in Berlin or Hamburg

Senior CRA - Phase I oncology trials - Hamburg/Berlin region

Associate Director (m/f/d), Computational Pathology Biomarker Lead (Oncology/BioPharma)

Country Study Manager

(Senior) Scientist (f/m/d) - Immunomonitoring

Manager FSP 360

Senior CRA

Senior CRA II Sponsor Dedicated based in Düsseldorf region

Global Senior Project Specialist (Sponsor Dedicated) Germany

More jobs to discover

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THE STUDY START UP ASSOCIATE ROLE

KEY RESPONSABILITIES

DESIRED QUALIFICATION & EXPERIENCE

TECHNICAL COMPETENCES & SOFT SKILLS

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