Aktiviere Job-Benachrichtigungen per E-Mail!

Associate Director Biostatistics Health Technology Assessment mwd Pharma Healthcare

DE50

München

Hybrid

EUR 80.000 - 120.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

Erhöhe deine Chancen auf ein Interview

Erstelle einen auf die Position zugeschnittenen Lebenslauf, um deine Erfolgsquote zu erhöhen.

Zusammenfassung

A leading global provider in healthcare analytics seeks a Director for their Biostatistics team. This role involves leading statistical analyses for HTA submissions, applying advanced methodologies, and mentoring junior staff. Flexible working options are available, including hybrid and remote arrangements.

Qualifikationen

  • Strong background in biostatistics with experience in HTA and programming.
  • Experience as a Director in a related field is preferred.

Aufgaben

  • Lead statistical analyses for AMNOG benefit assessments.
  • Produce and quality control statistical outputs.
  • Mentor and guide junior colleagues.

Kenntnisse

Biostatistics
Problem Solving
Attention to Detail
Statistical Methodologies

Ausbildung

MSc or PhD in Statistics
MSc or PhD in Biostatistics
MSc or PhD in Mathematics

Tools

R
SAS

Jobbeschreibung

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We provide actionable insights and deliver innovative solutions that improve patient outcomes and advance healthcare. Join us in driving healthcare forward.

Position: Director, Biostatistics (HEOR Team)

This position is an expert role focused on HTA-related programming and statistics. The successful candidate will lead statistical analyses for AMNOG benefit assessments in Germany and for EUHTA submissions, working closely with internal project teams and clients to ensure high-quality deliverables.

This role involves applying advanced statistical methodologies and programming to produce quality-controlled outputs. It offers flexible working arrangements, including a hybrid position in Munich or Frankfurt am Main, or fully remote with regular travel to Munich. A competitive salary and benefits package are provided.

Key Responsibilities:
  1. Apply innovative statistical approaches to address HTA-related data challenges.
  2. Lead analysis of patient data from clinical observational and real-world trials for HTA submissions.
  3. Develop and review HTA-related analysis plans.
  4. Produce and quality control statistical outputs, summaries, and reports.
  5. Provide statistical guidance to project teams and clients on HTA submissions.
  6. Engage with clients to understand project requirements and ensure satisfaction.
  7. Conduct feasibility assessments of evidence for HTA decision-making.
  8. Critically appraise data sources for quality and reliability.
  9. Mentor and guide junior colleagues.
  10. Contribute to internal training, process improvement, and business development initiatives.
Qualifications:
  • Strong background in biostatistics with experience in HTA and programming.
  • MSc or PhD in Statistics, Biostatistics, Mathematics, or a related field.
  • Understanding of clinical drug development, HTA regulations, and processes.
  • Familiarity with methodologies like NMA, ITC, and MAIC.
  • Proficiency in R and/or SAS.
  • Excellent problem-solving skills and attention to detail.
  • Ability to work independently and collaboratively.
  • Fluent in written and spoken English.
Additional Information:

We create connections to accelerate the development and commercialization of medical treatments to improve patient outcomes and population health worldwide. Learn more at our website.

Required Experience & Skills:

Experience as a Director in a related field is preferred. Key skills include expertise in computer science, mainframe, Active Directory, IT, ISO standards, Windows, ASP.NET, information security, Linux, project management, and related areas.

Employment Details:
  • Type: Full-Time
  • Location: Munich, Bavaria, Germany
  • Vacancies: 1
Hol dir deinen kostenlosen, vertraulichen Lebenslauf-Check.
eine PDF-, DOC-, DOCX-, ODT- oder PAGES-Datei bis zu 5 MB per Drag & Drop ablegen.