Statistical Programmer II

Evestia Clinical; Berlin; Hybrid; EUR 70.000 - 94.000; Vollzeit

Benefits dieser Stelle

Fully remote option

Berlin office collaboration days

Permanent contract

Competitive salary

Professional development

Zusammenfassung

Evestia Clinical in Berlin is seeking a Biostatistical Programmer II to join our growing European team. You will support the delivery of high-quality clinical trial data and statistical programming solutions, collaborating with internal and client project teams.

The role offers fully remote or hybrid-remote work with Berlin office collaboration days. Essential requirements include SAS programming and CDISC SDTM expertise, plus a Biostatistics background.

Qualifikationen

• Undergraduate degree in Biostatistics or related field.
• Experience in statistical programming for clinical research.
• Strong SAS programming and CDISC SDTM knowledge.
• Understanding regulatory requirements in clinical trials.

Aufgaben

• Collaborate with project teams to deliver high-quality data and programming outputs.
• Ensure SDTM datasets meet CDISC standards.
• Support UAT and data collection tools.

Kenntnisse

SAS programming

CDISC SDTM

Biostatistics

Clinical trials

Ausbildung

Bachelor's in Biostatistics

Jobbeschreibung

We are building something EPIC

We are building something EPIC
Evestia Clinical is a biotech-focused global CRO delivering authentic expertise and personalized support where client need it most.
Our foundation is built on four core principles: Innovation drives us to seek new solutions, Excellence defines the high standards we keep, and genuine Care ensures a supportive culture for both our patients and our people. We foster Partnership in everything we do, believing that working together—with trust and flexibility is the key to success.
Our approach is agile by nature and personalized by design. This translates to a workplace where you are empowered to find the creative solutions necessary for our collective success. We offer a welcoming, flexible, and supportive culture that values trust and belonging, ensuring you have the support needed to grow your skills and thrive while making a difference. We partner with our clients to provide expert knowledge and guidance through complex clinical trials in rare disease, oncology, neurology, immunology, and inflammation. At Evestia Clinical, you will become a vital part of a global specialist CRO. This means you will deliver life changing impact through clinical excellence.
We are committed to creating development opportunities that allow your skills to grow right alongside ours. If you are inspired by this collaborative environment and ready to change the lives of patients worldwide, we’d love to welcome you to our team.

About The Role

We are looking for a Biostatistical Programmer II to join our growing team in Europe and they will support the delivery of high-quality clinical trial data and statistical programming solutions. This role works closely with internal and client project teams, applying technical expertise to deliver compliant, high-quality outputs that contribute to the success of clinical research programmes.

What will your job look like?

• Work with the Project Team (e.g. Lead Statistician, Lead Data Manager and Project Manager), both internally and externally, to establish timelines, allocate resources, monitor budgets and resolve client, data and programming issues.
• Apply subject matter expertise in CDISC, Controlled Terminology and other applicable regulatory systems to project deliverables.
• Participate in internal and external team interactions and support the resolution of data and other project-related issues.
• Maintain awareness of budgets and projected hours required for assigned tasks.
• Contribute to the creation of data collection tools through User Acceptance Testing (UAT) and the provision of feedback.
  

What will you need to succeed?

• Undergraduate degree (or higher) in Biostatistics, Computer Science, or a related discipline.
• Experience in statistical programming within a clinical research environment.
• Strong knowledge of SAS programming.
• Experience working with CDISC standards, including SDTM.
• Understanding of applicable regulatory requirements and industry guidelines.
  

Our Offer

• Fully remote work or hybrid-remote with team collaboration days in our Berlin office.
• A supportive, diverse, and engaged team with flat hierarchies
• A permanent contract with a competitive salary and an attractive benefit package
• Active participation in professional development programs.
  

Our Commitment to Inclusion and Diversity

We are deeply proud of our people and the successes we achieve together. We actively seek out and hire individuals with diverse backgrounds, voices, beliefs, and perspectives to join our growing global workforce.

ICRC-Weyer is part of the Evestia Clinical Group of companies. They are an expert life science consultancy based in Berlin, Germany, with over 30 years of experience.

At ICRC-Weyer and Evestia Clinical, we believe that each person is unique. We celebrate your individuality, knowing that diverse viewpoints fuel Innovation and drive Excellence. We foster true Partnership across our global teams, guided by genuine Care for our colleagues. Our managers are dedicated to upholding this inclusive environment in every aspect of employment – from hiring and promotion to training and benefits.

It's who we are, it's what we do, it's what we care about.

Equal Opportunity & Accessibility

ICRC-Weyer and Evestia Clinical is an equal opportunity employer committed to diversity in the workplace. We ensure fair treatment of all applicants and employees, without discrimination based on actual or perceived race, color, creed, religion, national origin, age, sex, gender identity or expression, sexual orientation, disability, veteran status, or any other characteristic protected by applicable law.

We are committed to providing accessibility accommodations to applicants with physical and/or mental disabilities. If you are interested in applying for employment with the Evestia Clinical Group and require an accommodation or special assistance during the application process, please notify our recruitment team by sending an email with your request to [e-mail].