Posted: 14 April 2025
The Company
Our client is an Australian owned, private company specialising in the provision of Clinical Data Management services and deployment of eClinical solutions.
The Opportunity
As a Consultant Biostatistician, your role will be to support clients by providing expert biostatistical consulting, analysis, and oversight for their clinical trial activities. You will work closely with cross-functional teams to ensure statistical integrity, regulatory compliance, and high-quality deliverables across several therapeutic areas.
Main activities include:
- Providing Expert Consulting
- Data Analysis & Interpretation
- Protocal & SAP Development
- Regulatory Compliance & Documentation
- Cross-functional collaboration
- Mentorship & Oversight
The Requirements
- Minimum of 6+ years of experience in clinical trials or a related biostatistical consulting role for those with a PhD or 8+ years for those with a masters degree
- Proficiency with statistical software such as SAS, R, and/or other relevant tools.
- Expertise in statistical methodologies relevant to clinical trials, including survival analysis, mixed-effects models, Bayesian statistics, adaptive trial designs, and longitudinal data analysis.
- Deep understanding of regulatory requirements (e.g., FDA, EMA) and ICH guidelines.
- Strong problem-solving abilities with a proactive, solutions-oriented approach.
- Excellent written and verbal communication skills, with the ability to translate complex statistical information into clear, actionable insights for clients.
The Offer
This is an exciting opportunity to join a high-profile organisation in the Clinical Trials sector. Please email any questions you may have to Helen@purecdm.com.au.
To apply, please visit here to submit your current CV and cover letter.
