Senior Statistical Programmer

Metronomia; United Kingdom; Hybrid; GBP 60,000 - 90,000; Full time

Benefits offered by this job

Remote working options

Attractive remuneration and benefits

Flat hierarchy

Regular training opportunities

Job summary

METRONOMIA invites applications for a Senior Statistical Programmer in a globally oriented clinical research environment. The role involves programming and validating statistical analyses in SAS, and creating analysis datasets adhering to CDISC SDTM/ADaM standards.

Located in the UK, South Africa, or Germany with permanent residence in one of these countries, you will contribute to data management and medical writing projects while enjoying a remote-friendly, supportive team culture and ongoing

Qualifications

• 5+ years of professional experience in programming clinical studies.
• Strong SAS 9 programming skills; R experience a plus.
• CDISC SDTM and ADaM standards are mandatory.
• Degree in medical documentation, biometrics, statistics, mathematics or computer science.
• Fluent English communication.
• Personal initiative, reliability, enthusiasm and loyalty are required.

Responsibilities

• Program and validate statistical analysis of clinical studies with SAS.
• Define and program analysis datasets and CDISC SDTM and ADaM datasets in SAS.
• Quality control of evaluations of clinical studies.
• Conduct all other programming activities needed during a clinical study.

Skills

SAS programming

R knowledge

CDISC SDTM/ADaM

English communication

Professional reliability and ambition

Education

Degree in medical documentation / biometrics / statistics / mathematics / computer science

Tools

SAS 9

Job description

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 155 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

Senior Statistical Programmer

Location: UK, South Africa or Germany based (with a permanent residence in one of those countries)

Employment type: Full-time

Your responsibilities

1. You program and validate statistical analysis of clinical studies with SAS.
2. You define and program analysis datasets and CDISC SDTM and ADaM datasets in SAS.
3. You are responsible for the quality control of evaluations of clinical studies.
4. You conduct all other programming activities needed during a clinical study.

Your qualification

1. You have more than 5 years professional experience in programming activities of clinical studies (preferred in a Clinical Research Organisation or in the Pharmaceutical Industrie).
2. You have very good programming skills in SAS 9, experience in R would be a benefit.
3. Strong, hands-on application of CDISC SDTM and ADaM standards is mandatory for this role.
4. You have a degree in medical documentation, mathematical biometrics, statistics, mathematics, computer science or a comparable qualification.
5. You are communicative and carry out the required communication convincingly in English.
6. Personal initiative, reliability, enthusiasm and loyalty complete your profile.

Our offer for you

1. Appreciation and family-friendliness! We see and respect you as a person and support your professional compatibility with remote working models.
2. Excellence is worth it! We offer attractive remuneration and benefits!
3. 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!
4. 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!

If you have any questions in advance don't hesitate to contact our HR Managers Lachaé Leo ([e-mail]) or Christoph Hortian ([e-mail]).

Metronomia Clinical Research - www.metronomia.net

Metronomia is an equal opportunities employer. We welcome applications from all suitably qualified candidates and are committed to a fair and inclusive recruitment process. If you require any reasonable adjustments at any stage, please let us know.

Eligibility: To apply, you must already hold the right to work in the country where the role is based. This position is not eligible for visa sponsorship.