Senior Statistical Programmer - Oncology (m/w/d)

IQVIA, Inc.; Deutschland; Remote; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading global clinical research organization in Germany seeks an experienced Statistical Programmer to perform SAS programming for clinical studies. The role requires a Master's or Bachelor's degree in Biostatistics or related fields and 5+ years of experience in the CRO/Pharma sectors. Join a collaborative team, work on global projects, and help improve patient outcomes through innovative medical treatments.

Leistungen

Access to cutting-edge technology

Development opportunities

Collaborative work environment

Qualifikationen

• 5+ years of experience in Statistical Programmer role in CRO/Pharma.
• Experience in programming SDTM and ADaM datasets.
• Strong educational or practical evidence in programming.

Aufgaben

• Import data from various sources.
• Program quality control checks for source data.
• Write programming code following established Good Programming Practices.

Kenntnisse

SAS programming

Statistical analysis

Attention to detail

Problem solving

Organizational skills

Communication skills

Understanding of Good Clinical Practice

Ausbildung

Master's or Bachelor's degree in Biostatistics, Statistics, Mathematics, or Computer Science

Tools

SAS

Jobbeschreibung

Overview

IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based).

Responsibilities

• Import data from various sources
• Program quality control checks for source data and reporting data issues
• Interpret project level requirements and develop programming specifications
• Write programming code following established Good Programming Practices
• Program SDTM and ADaM datasets
• Program to create statistical analysis tables, listing and figures
• Validate datasets and all statistical outputs per prescribed gate checks
• Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines
• Use and promote the use of established standards, SOPs, and standard methodologies
• Export data and clinical study report materials
• Provide training and mentoring to team members and department staff

You can help us bring clinical trial statistical analysis into the next generation. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects across therapeutic areas. Be challenged in a fast-paced team environment that is collaborative in performing biostatistical analyses and advanced statistical programming. Development opportunities and mentoring at all levels enable you to progress your long-term career in the direction you choose.

THE PERSON

We know that meaningful results require not only the right approach, but also the right people. Candidates should possess a Master\'s or Bachelor\'s degree in Biostatistics, Statistics, Mathematics, or Computer Science, and have a strong educational or practical evidence in programming.

Key required skills

• Home Based/Remote
• 5+ experience in Statistical Programmer role from CRO/Pharma with ADaM/SDTM/ TLFs
• Excellent accuracy, attention to detail, problem solving, organizational as well as interpersonal communication
• In light of the above, candidates for the roles should exhibit the following skills and competencies
• Experience in programming in SAS within the CRO/Pharma/Biotech/Healthcare industries
• Knowledge of statistics and exhibit routine and occasionally complex analytical skills
• A focus on quality, accuracy, and completeness of work activities
• Excellent communication skills
• A good understanding of Good Clinical Practice and ICH guidelines
• Ability to independently lead (or have lead potential) and estimate programming scope of work, handle resource assignments, communicate work status, and work within project timelines for deliverables
• Take initiative and can be counted on to get the job done, with integrity
• Have the self-awareness to recognize when negotiating skills and assistance are needed
• Ability to establish and maintain effective working relationships with co-workers, managers, and clients

Embrace your curiosity and grow your career in an exciting environment where development is a priority. Think boldly and disrupt conventional thinking. Enjoy what you do. Discover a career with greater purpose and help create a healthier world.

This role is not eligible for UK visa sponsorship

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com