Dein persönlicher KI-Karriere-Agent
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.
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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
Ausbildung
Sprachen
Benefits
- Flexible working hours
- Flexible location
- Varied job
- Committed international team
- Modern infrastructure
- Supplementary vacation days
- Pension scheme contributions
- Internal skills training
- Support for continued education
Von Nejo automatisch aufbereitet
Nejo hat diesen Job automatisch von der Website des Unternehmens AO Foundation erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Zur Originalanzeige bei AO FoundationÜber das Unternehmen
The company is a not-for-profit organization specializing in the surgical treatment of trauma and musculoskeletal disorders.
aofoundation.orgNejo bewertet ihn, und bringt ihn danach gemeinsam mit dir in Bestform.
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