Clinical Statistical Programmer (Ii, Senior, Or Principal)

Clinical Statistical Programmer (Ii, Senior, Or Principal)
Company:

I-Pharm Consulting



Job Function:

Science

Details of the offer

Clinical Statistical Programmer (II, Senior, or Principal) We have an opportunity to join an award-winning, boutique Australian CRO as a Statistical Programmer (II, Senior, or Principal).

If you're looking for a shared learning environment and a genuine close-knit team, then here is your chance.
They have a genuinely positive working culture and push for shared learning and upskilling, so it's a great opportunity for anyone looking to develop cross-functional skills.

They have plans to grow in the coming years and so offer strong career progression opportunities as the team develops.
They are flexible with career growth and will work towards your own tailored pathways.

You will be working on full end-to-end projects and so skills in ADaM and SDTM are essential across a range of therapeutic areas - including oncology.

This role would suit anyone with 12 months of clinical statistical programming experience at a CRO or Pharmaceutical company.

KEY RESPONSIBILITIES Craft and validate SAS programs for comprehensive analysis and reporting of clinical trial data.
Collaborate intricately with statisticians, data managers, and peers to devise detailed statistical analysis plans.
Maintain meticulous documentation, ensuring adherence to regulatory standards and quality benchmarks.
Implement rigorous quality control measures to uphold data precision and uniformity.
Contribute to streamlining and enhancing standard programming procedures and tools.
Keep abreast of industry advancements, driving continuous enhancement.
DESIRED SKILLS: Hold a Bachelor's or Master's degree in statistics, computer science, or related fields.
Demonstrated expertise as a Clinical Statistical SAS Programmer within pharmaceutical, biotech, or clinical research sectors.
Proficiency in SAS programming, covering Base SAS, SAS/STAT, SAS Macro, and SAS/GRAPH.
Strong familiarity with CDISC standards and regulatory frameworks governing clinical trial data.
TITLE: Statistical Programmer (II, Senior, Principal) - Dependent on experience level
Location: Remote, Australia
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Source: Talent_Dynamic-Ppc

Job Function:

Requirements

Clinical Statistical Programmer (Ii, Senior, Or Principal)
Company:

I-Pharm Consulting



Job Function:

Science

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