We are seeking experienced Biostatisticians to join an award-winning clinical company - working 100% remote across Australia.
You will be responsible for managing multiple clinical trials, being the point of contact for statistical queries from sponsors, and helping mentor junior members of the team.
Being part of a smaller team means you will have more hands-on exposure and cross-functional responsibilities.
You will be working alongside industry professionals who have a collaborative approach, offering strong chances for progression and upskilling.
They offer fully flexible working and ensure a healthy workload across the team. People and culture are a huge priority for this business, and it continues to remain throughout their growth.
They have some really interesting project scopes, partnering with a range of niche Biotechnology and Pharmaceutical sponsors - working on various therapeutic areas, including complex oncology.
This role would suit an experienced Biostatistician (3+ years) with extensive clinical trial experience.
Responsibilities:
Provide statistical guidance throughout the lifecycle of clinical studies, including study design, sample size calculations, randomization, and analysis. Develop and write comprehensive statistical analysis plans (SAPs) that outline the methodology for data analysis. Conduct statistical analyses, interpret results, and present findings to stakeholders, ensuring clarity and understanding of complex data. Work closely with cross-functional teams including clinical operations, data management, and regulatory affairs to ensure alignment on study objectives and outcomes. Monitor and verify statistical programming tasks performed by junior statisticians or programmers, ensuring accuracy and compliance with regulatory standards. Prepare integrated clinical study reports and contribute to the preparation of regulatory submissions. Engage with clients to understand their statistical needs, provide recommendations, and educate them on statistical methodologies. Qualifications:
Degree in Statistics, Biostatistics, Mathematics, or a related field; PhD is a plus. Minimum of 3 years of experience in the pharmaceutical or CRO industry with a focus on clinical trials. Proficiency in statistical software such as SAS or R; familiarity with programming languages for data manipulation is an advantage. Must have CDISC knowledge. Excellent verbal and written communication skills to convey statistical concepts to non-statistical audiences. Location: Remote, Australia
Salary: $110,000 - $160,000 - open to negotiate for experienced candidates.
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