Clinical Data Programmer Iii Sas

**About the role**:
The Clinical Data Programmer SAS III (must be SAS Certified) is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating reports, visualizations, and dashboards for Clinical Data Managers (CDM), Clinical Data Reviewers (CDR), Project Managers (PM) and other clinical study stakeholders.

**Minimum Qualifications & Experience**:

- Must be SAS Certified
- Graduate in computer science, data science, mathematics, or life science related field, or similar.
- A minimum of 10 years of experience in a role related to business intelligence, data science, data analysis, and clinical data management or clinical data programming in a pharmaceutical company, CRO or EDC software provider.
- Familiar with Business Intelligence tools to interrogate clinical and laboratory datasets (e.g. TIBCO Spotfire, Power BI), and/or statistical software.
- Good knowledge of clinical study data structures and schemas of EDC databases.
- Statistical programming skills in SAS, Python, R or similar.
- Knowledge of SQL and EDC systems and familiar with TIBCO Spotfire, Power BI, Tableau, or other data review and visualisation tool.

**Responsibilities**:
The Clinical Data Programmer SAS III is responsible for assisting clinical study teams and other stakeholders to deliver data visualisations (Graphs/Dashboards) and reports (Tables, Listings) using Business intelligence/ Clinical Data Visualisation tools

1.Project/Clinical Studies
- Work under supervision as Clinical Data Programmer SAS gathering clinical and external data reporting and visualisation user requirements from CDMs, CSRs, PMs, and other study stakeholders to facilitate data inspection, data reconciliation, and clinical review, and provide guidance on appropriate output formats (dashboards, visualisations, listings, reports).
- Document user requirements and undertake programming of the data visualisations (Graphs/Dashboards) and reports (Tables, Listings) using prototyping techniques and ensure the final programs are validated as they move through the development stages (DEV, UAT, PROD), as per applicable procedures.
- Educate and train the users of the data visualisations (Graphs/Dashboards) and reports (Tables, Listings) on how to use all the features in the data visualisation software platform to inspect and explore the data and make business decisions.
- Extract, assess, integrate, transform clinical study data from EDC and other sources during study conduct to provide the data visualisation outputs to the study users, i.e. CDMs, CSRs, PMs and others.

2. Clinical Data Visualisation Team
- Participate in Clinical Data Visualisation team and Biometrics department meetings.

3. Software Tools
- Develop proficiency with Business Intelligence, Clinical Data Visualisation tools and SAS software.

4. Clinical Data Visualisation Processes and SOPs
- Ensure compliance with Novotech' s corporate SOPs and applicable regulatory guidelines.
- Adhere to SOPs and best practice instructions and templates related to clinical data visualisation

Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.

Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.

We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.