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Director Statistical Programming (Oncology)(m/w/x)
Beschreibung
You lead statistical programming efforts, ensuring high-quality data analysis and regulatory compliance while collaborating with various teams to optimize processes and improve efficiency in clinical trials.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Bachelor’s degree in Statistics or related discipline
- •15+ years experience in pharmaceutical industry
- •Excellent knowledge of statistical programming in SAS
- •Solid understanding of FDA and global regulations
- •Solid understanding of CDISC standards
- •Solid understanding of drug development process
- •Expertise in electronic submissions technology
- •Strong interpersonal and communication skills
- •Strong analytical and problem-solving skills
- •Ability to work in a fast-paced environment
Ausbildung
Berufserfahrung
15 Jahre
Aufgaben
- •Implement strategies to enhance statistical analysis efficiency.
- •Oversee FSP programmers and vendor CROs for timely delivery.
- •Align programming with regulatory requirements and objectives.
- •Drive creation and validation of SAS/R programs for analysis.
- •Ensure compliance with SOPs and regulatory standards.
- •Collaborate with teams to shape study designs and analysis plans.
- •Represent programming in clinical study team meetings.
- •Lead programming for global regulatory submissions.
- •Manage production of submission-ready datasets and documentation.
- •Promote advanced analytics and automation tools for efficiency.
- •Develop standardized processes and mentor teams on trends.
- •Establish innovative solutions to enhance statistical reporting.
- •Participate in continuous improvement for clinical initiatives.
Tools & Technologien
Benefits
Mentale Gesundheitsförderung
- •Commitment to team wellbeing
Attraktive Vergütung
- •Competitive remuneration packages
- BioNTech SEVollzeitnur vor OrtSeniorMainz
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Director Statistical Programming (Oncology)(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
You lead statistical programming efforts, ensuring high-quality data analysis and regulatory compliance while collaborating with various teams to optimize processes and improve efficiency in clinical trials.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Bachelor’s degree in Statistics or related discipline
- •15+ years experience in pharmaceutical industry
- •Excellent knowledge of statistical programming in SAS
- •Solid understanding of FDA and global regulations
- •Solid understanding of CDISC standards
- •Solid understanding of drug development process
- •Expertise in electronic submissions technology
- •Strong interpersonal and communication skills
- •Strong analytical and problem-solving skills
- •Ability to work in a fast-paced environment
Ausbildung
Berufserfahrung
15 Jahre
Aufgaben
- •Implement strategies to enhance statistical analysis efficiency.
- •Oversee FSP programmers and vendor CROs for timely delivery.
- •Align programming with regulatory requirements and objectives.
- •Drive creation and validation of SAS/R programs for analysis.
- •Ensure compliance with SOPs and regulatory standards.
- •Collaborate with teams to shape study designs and analysis plans.
- •Represent programming in clinical study team meetings.
- •Lead programming for global regulatory submissions.
- •Manage production of submission-ready datasets and documentation.
- •Promote advanced analytics and automation tools for efficiency.
- •Develop standardized processes and mentor teams on trends.
- •Establish innovative solutions to enhance statistical reporting.
- •Participate in continuous improvement for clinical initiatives.
Tools & Technologien
Benefits
Mentale Gesundheitsförderung
- •Commitment to team wellbeing
Attraktive Vergütung
- •Competitive remuneration packages
Über das Unternehmen
BioNTech SE
Branche
Pharmaceuticals
Beschreibung
BioNTech focuses on advancing innovative therapies for cancer and infectious diseases. The company is committed to excellence in research and development, with a strong emphasis on collaboration and cutting-edge technology.
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Associate Director Clinical Trials(m/w/x)
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