Current jobs related to Senior Biostatistician - Melbourne, Victoria - Avance Clinical Pty


  • Melbourne, Victoria, Australia Pharmiweb Full time

    Senior Biostatistician - Clinical Trials Expert ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to be a part of our mission to shape the future of clinical development.Key Responsibilities:Design and analyze clinical...

Senior Biostatistician

2 months ago


Melbourne, Victoria, Australia Avance Clinical Pty Full time
Senior Biostatistician Opportunity

We are seeking a highly skilled Senior Biostatistician to join our team at Avance Clinical Pty. As a key member of our biostats team, you will play a critical role in the design, analysis, and interpretation of clinical trials.

Key Responsibilities
  • Develop and review statistical analysis plans and randomization schedules to ensure high-quality data.
  • Prepare and review listings, tables, and figures for interim analyses and clinical study reports to facilitate informed decision-making.
  • Perform complex statistical analyses to identify trends and patterns in data.
  • Review CDISC SDTM and ADaM specification documents to ensure compliance with regulatory requirements.
  • Collaborate with Clinical Project Managers, Data Management team, and external vendors to ensure seamless study execution.
  • Communicate effectively with clients to discuss study processes, timelines, and results.
  • Review Case Report Forms for data capture and monitor study budgets to identify potential issues.
Requirements
  • Ordinary degree in a relevant discipline or equivalent industry experience.
  • Higher degree in Biostatistics or a related field to drive scientific research and data analysis.
  • Minimum 5 years of experience in statistical analysis in pharmaceutical or health research.
  • Working knowledge of ICH GCP Guidelines, medical terminology, and clinical trials processes.
  • SAS programming experience is highly desirable.
  • Working knowledge of CDISC SDTM and ADaM implementation and requirements is highly desirable.
  • Understanding of pharmacokinetics is desirable.
  • Excellent communication and interpersonal skills to work effectively with clients and stakeholders.
  • Ability to work under pressure in a fast-paced, multi-disciplinary team environment.
What We Offer
  • A reputable and growing CRO with a stable and supportive work environment.
  • A challenging and stimulating role where your expertise makes a real difference.
  • A diverse and inclusive culture that values collaboration and teamwork.
  • Opportunities for training and career development to help you grow professionally.
  • Attractive remuneration and flexible work arrangements to suit your needs.

Please submit your application, including your CV and a cover letter outlining your skills and experience, as a single PDF document. Full Australian working rights are required for this role. No agencies, please.