Statistical Programmer* (located in United Kingdom)

Metronomia Clinical Research GmbH; London; Remote; GBP 40,000 - 60,000; Full time

Job summary

Une entreprise dynamique dans le secteur de la recherche clinique recherche un Programateur Statistique pour rejoindre son équipe au Royaume-Uni. Le candidat idéal aura une expérience en programmation SAS et sera responsable de la programmation et de la validation d'analyses statistiques pour des études cliniques. Avec un environnement de travail convivial et familial, cette entreprise offre une rémunération compétitive et des opportunités de développement professionnel.

Benefits

Modèles de travail à distance

Rémunération attractive

Formation continue

Qualifications

• Expérience professionnelle dans les études cliniques.
• Compétences avancées en programmation SAS.
• Connaissances des normes CDISC SDTM et ADaM.

Responsibilities

• Programmer et valider l'analyse statistique des études cliniques avec SAS.
• Définir et programmer les ensembles de données d'analyse dans SAS.
• Contrôler la qualité des évaluations d'études cliniques.

Skills

Programmation en SAS

Analyse statistique

Communication en anglais

Education

Diplôme en biométrie médicale, statistiques ou informatique

Job description

Statistical Programmer* (located in United Kingdom)

Metronomia Clinical Research GmbH

City Of London

GBP 40,000 - 60,000

Since 1990, METRONOMIA has stood for quality, competence, continuity and unconditional customer orientation in terms of data management, statistical services and medical writing in clinical research. As a growth-oriented medium-sized company with over 145 employees, we operate internationally. Our customers appreciate the competence and commitment of our employees and we value our employees as the basis of the company's success. Join a motivated and friendly team as

Statistical Programmer

(UK Remote)

Your responsibilities

• You program and validate statistical analysis of clinical studies with SAS.
• You define and program analysis datasets and CDISC SDTM and ADaM datasets in SAS.
• You are responsible for the quality control of evaluations of clinical studies.
• You conduct all other programming activities needed during a clinical study.
• You have professional experience in programming activities of clinical studies.
• You have very good programming skills in SAS 9, experience in R would be a benefit.
• You have gained practical experience with CDISC SDTM and ADaM standards.
• You have a degree in medical documentation, mathematical biometrics, statistics, mathematics, computer science or a comparable qualification.
• You are communicative and carry out the required communication convincingly in English. Knowledge of German is an advantage.
• Personal initiative, reliability, enthusiasm and loyalty complete your profile.

Our offer for you

• Appreciation and family-friendliness! We see and respect you as a person and support your professional compatibility with remote working models.
• Excellence is worth it! We offer attractive remuneration and benefits!
• Flat hierarchy! Our entire team meets at eye level at all times! In this way, we create a special working atmosphere for our highly motivated and qualified team!
• Challenging tasks! There is a detailed introduction to the area of responsibility and regular opportunities for internal and external training!

Have we piqued your interest? We look forward to getting to know you!

Please send us your CV or your LinkedIn profile including details of your possible start date and salary expectations. If you have any questions about the position and the application process, please do not hesitate to contact our HR Manager Christoph Hortian (+49 - 89 - 829 265 101 / [e-mail]).