Sr. Scientist, Stat. Programming (m/f/d)

Merck

Oudergem

Sur place

EUR 75 000 - 120 000

Plein temps

Il y a 2 jours
Soyez parmi les premiers à postuler
Générateur de candidature

Obtenez une réponse de cet employeur — un CV et une lettre de motivation adaptés exactement à ce qu’on recherche pour ce poste.

Passez les filtres ATS

Résumé du poste

Merck in Brussels is seeking a Senior Statistical Programmer, Health Technology Assessment (HTA) to develop statistical programming activities for HTA dossiers and enable fair patient access to medicines and vaccines.

You will define and implement strategic solutions using multiple programming languages to create analysis datasets, tables, listings and figures from clinical trial data, collaborating with HTA biostatisticians and stakeholders.

Qualifications

  • BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related analytical field plus 5-9 years programming experience in R and/or SAS.
  • MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related analytical field plus 3-7 years in R and/or SAS programming experience.
  • Significant expertise in R and SAS clinical trial programming including data processing, statistical procedures and graphing and tabulation techniques; systems and database expertise.
  • Working knowledge of statistics, clinical and data management concepts as applied to drug/vaccine development within the pharmaceutical industry.
  • Knowledge in CDISC SDTM and ADaM standards.
  • Effective knowledge and experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings).
  • Business fluency in English (oral and written).
  • A project leader; completes tasks independently at a project level; ability to collaborate with key stakeholders.
  • Ability to quickly and effectively learn new program techniques and data structures; capacity to assimilate to new projects.
  • Ability to comprehend analysis plans which may describe HTA research and statistical programming methodology.
  • Experience ensuring process compliance and deliverable quality.
  • Strategic thinking - ability to turn strategy into tactical activities; design of statistical databases with the end in mind.
  • Team oriented with demonstrated history of teamwork and collaboration across cultures.

Responsabilités

  • Programmatically develop, validate and maintain analysis and reporting deliverables for HTA dossiers.
  • Provide statistical programming project leadership to key project dimensions.
  • Ensure deliverable quality and compliance with SOPs and good programming practices.
  • Collaborate effectively with project team members; be a valued part of project teams.
  • Membership on departmental strategic initiative teams.

Connaissances

AI Programming
Data Analysis in R
Numerical Analysis
R Programming
SAS Language
Statistical Analysis
Statistical Programming

Formation

BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related analytical field plus 5-9 years programming experience in R and/or SAS
MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related analytical field plus 3-7 years in R and/or SAS programming experience

Outils

R
SAS

Description du poste

Job Description

Our Quantitative Sciences team use big data to analyze the safety and efficacy claims of our potential medical breakthroughs. We review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality data to support decision making in clinical trials. Our Biostatistics and Research Decision Sciences (BARDS) organization has a presence in the US, EU and Asia Pacific and a proud record of providing comprehensive analytical and methodological expertise to support our company's strategic goals.

We offer long-term career opportunities in a company which values innovation, efficiency, diversity and respect. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork.

As an addition to our BARDS Team and located in our office in Brussels, we are currently looking for a Senior Statistical Programmer, Health Technology Assessment (m/f/d) ( full-time, indefinite ) to develop statistical programming activities focusing on the analysis and reporting needs for Health Technology Assessment (HTA) dossiers; with the goal to provide fair accessibility for patients to our company's medicines and vaccines, making a real difference in patient's lives.

On this role you will contribute to the definition and implementation of strategic solutions utilizing multiple programming languages to create analysis datasets, tables, listing and figures from clinical trial data. You will be a key collaborator with HTA biostatisticians and other project stakeholders in ensuring that project plans are executed efficiently with timely and high-quality deliverables. As a senior programmer you will be the point of contact and for assigned projects and will also perform development and validation activities following departmental SOPs.

THE PRIMARY ACTIVITIES INCLUDE BUT ARE NOT LIMITED TO:
  • Programmatically develop, validate and maintain analysis and reporting deliverables for HTA dossiers.
  • Ensure proper project planning; provide statistical programming project leadership to key project dimensions.
  • Assure deliverable quality and compliance with departmental SOPs and good programming practices.
  • Collaborate effectively with project team members; be a valued part of project teams.
  • Membership on departmental strategic initiative teams.
QUALIFICATIONS:
  • BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related analytical field plus 5-9 years programming experience in programming languages like R and/or SAS Or
  • MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related analytical field plus 3-7 years in R and/or SAS programming experience
  • Significant expertise in R and SAS clinical trial programming including data processing, statistical procedures and graphing and tabulation techniques; systems and database expertise.
  • Working knowledge of statistics, clinical and data management concepts as applied to drug/vaccine development within the pharmaceutical industry.
  • Knowledge in CDISC SDTM and ADaM standards.
  • Effective knowledge and experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings).
  • Business fluency in English (oral and written).
  • A project leader; completes tasks independently at a project level; ability to collaborate with key stakeholders.
  • Ability to quickly and effectively learn new program techniques and data structures; capacity to seamlessly assimilate to new projects.
  • Ability to comprehend analysis plans which may describe HTA research and statistical programming methodology to be programmed; an understanding of statistical terminology and concepts.
  • Experience ensuring process compliance and deliverable quality.
  • Strategic thinking - ability to turn strategy into tactical activities; design of statistical databases with the end in mind that optimize analysis and reporting and leverage departmental standards and industry best-practices.
  • Team oriented with demonstrated history of teamwork and collaboration across cultures and geographies; enjoying diversity, respect and integrity.

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we "follow the science" that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

Required Skills:
  • AI Programming, Data Analysis in R, Numerical Analysis, Project Scoping, R Programming, SAS Language, Statistical Analysis, Statistical Programming
Current Employees
Obtenez votre examen gratuit et confidentiel de votre CV.

ou faites glisser et déposez votre fichier ici.

Similar jobs

Postes similaires à comparer

Sr. Scientist, Stat. Programming (m/f/d)
Sr. Scientist, Stat. Programming (m/f/d)

CamWebDir • Brussel Hoofdstad

Hybride
GBP 65 000 - 82 000
Sr. Scientist, Stat. Programming (m/f/d)
Sr. Scientist, Stat. Programming (m/f/d)

MSD Malaysia • Brussel Hoofdstad

Sur place
EUR 80 000 - 110 000
Hybrid work arrangements
Sr. Scientist, Stat. Programming (m/f/d)
Sr. Scientist, Stat. Programming (m/f/d)

MSD Belgium • Brussel Hoofdstad

Sur place
EUR 65 000 - 95 000
Associate Biostatistics Director - FSP (Permanent Home-based)
Associate Biostatistics Director - FSP (Permanent Home-based)

IQVIA • Brussel

Sur place
EUR 90 000 - 130 000
Associate Biostatistics Director - FSP (Permanent Home-based)
Associate Biostatistics Director - FSP (Permanent Home-based)

IQVIA • Zaventem

Sur place
EUR 110 000 - 165 000
Principal Biostatistician (Integrated analysis experience required) EU based
Principal Biostatistician (Integrated analysis experience required) EU based

Syneos Health • Belgique

Sur place
EUR 90 000 - 150 000
Senior Statistical Programmer, HTA – Data & Impact Leader
Senior Statistical Programmer, HTA – Data & Impact Leader

Merck • Oudergem

Sur place
EUR 75 000 - 120 000
Senior Statistical Programmer - HTA (R/SAS) | Hybrid
Senior Statistical Programmer - HTA (R/SAS) | Hybrid

MSD Malaysia • Brussel Hoofdstad

Hybride
EUR 80 000 - 110 000
Hybrid work arrangements
Principal C&SP Methodology Lead
Principal C&SP Methodology Lead

Johnson & Johnson Innovative Medicine • Gierle

Sur place
EUR 110 000 - 160 000
Senior Principal Programmer (Belgium)
Senior Principal Programmer (Belgium)

UCB • Brussel

Hybride
EUR 120 000 - 160 000