Principal Biostatistician - Melbourne, Australia - I-Pharm Consulting
Description
A Contract Research Organisation (CRO), is actively seeking a Principal Biostatistician to lead their statistical division. This role encompasses both project-based oversight and team leadership responsibilities, necessitating adept communication skills for liaising with sponsors and internal stakeholders.
This presents an opportunity to lead a dedicated team of statisticians within a small-mid sized CRO that places premium value on innovation, collaboration, and client contentment. They offer an enticing salary package, a nurturing work milieu, and avenues for professional advancement. If you possess a fervour for statistics, clinical research, and aspire to leave a profound mark in the healthcare sector, we encourage you to submit your application.
Company Profile:
This CRO is a committed provider of top-tier clinical research services to pharmaceutical, biotechnology, and medical device enterprises. Their personalised approach and unwavering commitment to excellence ensure the delivery of invaluable insights and solutions to intricate projects spanning various therapeutic domains.
Position: Principal Biostatistician
Location: AU (remote)
Salary: Enhanced salary packages available - To Be Confirmed (TBC)
Responsibilities:
Lead and oversee the statistical team, providing mentorship, guidance, and fostering a culture of collaboration and innovation. Supervise the statistical aspects of clinical trials and research initiatives, ensuring utmost accuracy and compliance with pertinent regulations and industry benchmarks. Collaborate with cross-functional teams to devise and refine appropriate statistical methodologies for study protocols, sample size calculations, randomisation, and analysis plans. Execute statistical analyses, decipher findings, and contribute to the formulation of study reports, regulatory submissions, and publications. Review and validate statistical outputs, ensuring data integrity and quality. Stay abreast of industry developments, trends, and regulatory alterations in statistical methodologies, contributing to the ongoing enhancement of processes and best practices within the organisation. Offer statistical insights during client interactions, cultivating robust client relationships, and ensuring client satisfaction. Requirements:
Bachelor's degree in Statistics, Biostatistics, or a related field. Demonstrated experience (minimum 3 years) in statistical analysis within the pharmaceutical, biotechnology, or CRO sector. Proficient knowledge of clinical trial design, methodologies, and regulatory guidelines (ICH, FDA, etc.). Ability to convey statistical concepts and findings effectively to both technical and non-technical audiences. Strong problem-solving aptitude and meticulous attention to detail. How to Apply:
Apply directly for the position via this link or send your CV to Keeley Munday at - Alternatively, you can call directly on
Associated Keywords: Statistics Manager, CRO (Contract Research Organisation), Clinical Research, Statistician, Biostatistics, Pharmaceutical, Biotechnology, Medical Device, Statistical Analysis, Statistical Methodologies, Study Design, Data Analysis, SAS, R, SPSS, Regulatory Guidelines, ICH (International Council for Harmonisation), FDA (U.S. Food and Drug Administration), Clinical Trials, Adaptive Clinical Trials, Bayesian Statistics, Leadership, People Management, Team Management, Communication Skills, Business Development, Client Relationship, Mentorship