AO Foundation
Senior Project Manager Clinical Operations(m/w/x)
Vollzeit/Teilzeitmit HomeofficeSenior
Zizers
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AOAO Foundation
Clinical Research Associate(m/w/x)
Zizers
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Managing clinical studies for surgical treatment research, ensuring GCP adherence and investigator integrity. Structured, detail-oriented working style required. Flexible working hours and location, committed international team.
Anforderungen
- Strong communication skills (written and verbal)
- Structured, detail-oriented working style
- Reliable documentation
- Ability to prioritize tasks
- Ability to manage multiple tasks
- Ability to meet deadlines
- Collaborative team player
- Proactive, solution-oriented mindset
- Independent task performance using guidelines
- Support department goal achievement
- Bachelor in Natural Science or nursing degree
- Further education in Clinical Research
- Work experience as Clinical Research Associate
- Good market and product knowledge
- Basic medical knowledge
- Good understanding of study-related outcome measures
- Experience with data capture in clinical research
- Strong organizational skills
- Strong follow-up skills
- Attention to detail
- Reliability
- Ability to work independently
- Ability to work in a team
- Flexibility
- Customer-focused mindset
- Strong written communication skills in English
- Strong oral communication skills in English
- English or German language skills
Aufgaben
- Manage clinical studies under scientific and legal guidelines
- Collaborate with project leaders on study management
- Prepare and conduct site evaluations, initiations, monitoring, and close-outs
- Ensure GCP adherence and investigator integrity
- Plan short and long-term monitoring to ensure data quality and compliance
- Prepare and submit documents to public authorities and ethics commissions
- Develop and adapt Case Report Forms (CRFs)
- Control quality and collection of clinical data
- Update Project Managers on documentation quality and site status
- Implement solutions to maintain or adapt project timelines, budget, and scope
- Maintain contact with Principal Investigators and Study Coordinators
- Provide support to conduct clinical investigations
- Conduct regular trainings for study sites
- Prepare and develop Study Newsletters and annual reports
- Prepare clinical data for analysis with the project team
- Assist in optimizing quality standards and SOPs
- Prepare, assist, and coordinate contract negotiations
- Perform tasks in alignment with ISO 9001 quality management standards
- Contribute to maintaining and improving the quality system
- Undertake additional responsibilities as assigned by the line manager
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Benefits
Flexibles Arbeiten
- Flexible working hours
- Flexible location
Abwechslungsreiche Aufgaben
- Varied job
Lockere Unternehmenskultur
- Committed international team
Modernes Büro
- Modern infrastructure
Mehr Urlaubstage
- Supplementary vacation days
Betriebliche Altersvorsorge
- Pension scheme contributions
Weiterbildungsangebote
- Internal skills training
- Support for continued education
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