Dein persönlicher KI-Karriere-Agent
Principal Statistician(m/w/x)
Statistical analysis for clinical trials, developing study protocols, and training statisticians at a global CRO. Expert knowledge of SAS programming and CDISC ADaM standard required. Mentoring opportunities for junior statisticians.
Anforderungen
- MSc in Statistics or equivalent
- Full working proficiency in English
- Expert knowledge of statistical principles
- Expert knowledge of SAS programming
- Expert knowledge of CDISC ADaM standard
- Expert knowledge of adaptive designs
- Expert knowledge of sample size calculation
- Expert knowledge of relevant regulations
- Ability to apply advanced statistical techniques
- Ability to consult with clinical investigators
- Strong presentation and communication skills
Aufgaben
- Serve as a communication link for project teams and clients.
- Conduct statistical analysis for clinical trials.
- Develop and review study protocols and analysis plans.
- Review statistical deliverables like tables and datasets.
- Conduct training for statisticians and SAS programmers.
- Prepare for and attend study audits related to statistics.
- Participate in follow-up for internal/external audits.
- Provide input to standard operating procedures for Biostatistics.
- Liaise with data management on statistical data issues.
- Participate in bid defense and kick-off meetings.
- Lead teams of SAS programmers and statisticians.
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- SAS
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Principal Statistician(m/w/x)
Statistical analysis for clinical trials, developing study protocols, and training statisticians at a global CRO. Expert knowledge of SAS programming and CDISC ADaM standard required. Mentoring opportunities for junior statisticians.
Anforderungen
- MSc in Statistics or equivalent
- Full working proficiency in English
- Expert knowledge of statistical principles
- Expert knowledge of SAS programming
- Expert knowledge of CDISC ADaM standard
- Expert knowledge of adaptive designs
- Expert knowledge of sample size calculation
- Expert knowledge of relevant regulations
- Ability to apply advanced statistical techniques
- Ability to consult with clinical investigators
- Strong presentation and communication skills
Aufgaben
- Serve as a communication link for project teams and clients.
- Conduct statistical analysis for clinical trials.
- Develop and review study protocols and analysis plans.
- Review statistical deliverables like tables and datasets.
- Conduct training for statisticians and SAS programmers.
- Prepare for and attend study audits related to statistics.
- Participate in follow-up for internal/external audits.
- Provide input to standard operating procedures for Biostatistics.
- Liaise with data management on statistical data issues.
- Participate in bid defense and kick-off meetings.
- Lead teams of SAS programmers and statisticians.
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- SAS
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
PSI CRO
Branche
Pharmaceuticals
Beschreibung
The company is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation.
Noch nicht perfekt?
- PSI CRO
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