Senior Principal Statistical Programmer

Stelle nicht auf LinkedIn

🕒 vor 5 Tagen

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $131.100 - $160.000 / Jahr

⏰ Vollzeit

🟠 Senior

🖥 Softwareentwickler

Jetzt Bewerben

Ähnliche Remote-Jobs finden

E-Mail-Benachrichtigung für neue Jobs einrichten

📊 Überprüfen Sie Ihre Lebenslauf-Bewertung für diese Stelle

Verbessern Sie Ihre Chancen auf ein Vorstellungsgespräch, indem Sie Ihre Lebenslauf-Bewertung vor der Bewerbung überprüfen.

Lebenslauf hochladen

WCG

WebsiteLinkedInAlle Stellen

1001 - 5000 Mitarbeiter

🏥 Gesundheitswesen

💊 Pharmazie

☁️ SaaS

💰 Private Equity Round - WCG im 2019-11

Healthcare • Pharmaceuticals • SaaS

WCG ist ein globales Unternehmen für klinische Forschungsdienstleistungen und -technologie, das Sponsoren, CROs, Forschungsstellen und Institutionen während des gesamten Lebenszyklus klinischer Studien unterstützt. Gegründet als ein führendes Unternehmen im Bereich unabhängiger ethischer Prüfungen, bietet WCG IRB- und IBC-Prüfungen, Datenüberwachungskomitees, Standortaktivierung und Studienstartdienste, Teilnehmerrekrutierung und -bindung sowie Daten & Einblicke (einschließlich Benchmarking, Statistikberatung und KI-gestützte Studienvorausschau). Das Unternehmen bietet auch eine Reihe von Technologieplattformen (z. B. ClinSphere®, eReview Manager, Total Enrollment, Total Feasibility) und große Protokoll- und Leistungsdatensätze, um Studien effizienter und konformer zu gestalten, zu planen und durchzuführen. WCG positioniert sich als Partner für biopharmazeutische und medizinische Forschungsorganisationen, um die Aktivierung von Studien zu beschleunigen, die Rekrutierung zu verbessern und die regulatorische und ethische Compliance sicherzustellen.

Beschreibung

• Serve as a senior technical expert in statistical programming, providing guidance across multiple studies or functional areas. • Design, develop, validate, and oversee complex statistical programming deliverables, including analysis datasets, tables, listings, and figures. • Lead the development, validation, and continuous improvement of DMC macros and programming standards. • Provide technical oversight and review of programming work to ensure quality, compliance, and consistency across deliverables. • Drive the establishment and adoption of programming standards, best practices, and process improvements. • Collaborate with biostatistics and study teams to support complex trial designs, analyses, and DMC reporting. • Independently manage and prioritize programming activities across multiple studies or initiatives. • Mentor and provide technical leadership to statistical programming staff, supporting skill development and best practices. • Contribute technical expertise to proposals, project planning, and scope discussions as needed. • Partner with IT and technology teams to support SAS environments, tools, and system validation efforts. • Provide technical oversight for programming activities supporting regulatory submissions and inspection readiness. • Ensure programming deliverables align with regulatory expectations, submission requirements, and CDISC standards. • Influence programming approaches, standards, and best practices across multiple studies or programs. • Serve as a technical escalation point for complex programming, data, or deliverable issues, leading resolution of highly complex or ambiguous challenges. • Provide expert interpretation of statistical analysis plans (SAPs), protocols, and study documents, translating requirements into programming strategy. • Champion process improvements, automation, and innovative approaches to enhance efficiency, scalability, and consistency of programming deliverables. • Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.

🎯 Anforderungen

• Minimum 8–10 years of statistical programming experience in a clinical trial environment • Deep expertise in SAS programming, including complex analyses and regulatory deliverables • Proficiency in R programming is a must • Demonstrated experience with CDISC standards and regulatory requirements • Proven ability to independently lead complex programming efforts across studies • Experience mentoring staff and driving technical standards or best practices • Demonstrated ability to independently coordinate biostatistical projects, including planning and oversight of programming activities, with minimal direction from senior leadership.

🏖️ Vorteile

• Comprehensive Benefits package - Health, Dental, Vision, Life Disability, 401k with match, and flexible spending accounts • Employee Assistance Programs and additional work/life resources • Referral Bonuses and Tuition Reimbursement • Flexible PTO • Volunteer Time Off to benefit the community • Opportunities for career development with on-the-job training, certification assistance, and continuing education reimbursement