We have a current opportunity for a AD Biostatistics on a permanent basis. The position will be based in New Jersey (3x a week). For further information about this position please apply.
Job Title: Associate Director of Biostatistics
Location: New Jersey, USA 3x a week on site
Company Overview: We are a dynamic and innovative biotech company focused on developing cutting-edge therapies in the fields of oncology and central nervous system (CNS) disorders. Our mission is to bring life-changing treatments to patients through rigorous scientific research and clinical excellence.
Position Summary: The Associate Director of Biostatistics will play a pivotal role in our clinical development programs, providing statistical leadership and expertise in the design, analysis, and interpretation of clinical trials. This position will collaborate closely with cross-functional teams to ensure the integrity and accuracy of our clinical data, ultimately supporting the advancement of our oncology and CNS pipelines.
Key Responsibilities:
- Lead the statistical design, analysis, and reporting of clinical trials in oncology and CNS.
- Develop and review statistical analysis plans (SAPs) and ensure compliance with regulatory requirements.
- Provide statistical input into clinical development plans, study protocols, and regulatory submissions.
- Collaborate with clinical, regulatory, and data management teams to ensure high-quality data collection and analysis.
- Oversee the work of biostatisticians and statistical programmers, providing mentorship and guidance.
- Conduct exploratory data analyses and support the development of publications and presentations.
- Stay current with industry trends and advancements in biostatistics and clinical trial methodologies.
Qualifications:
- Ph.D. or M.S. in Biostatistics, Statistics, or a related field.
- Minimum of 5 years of experience in biostatistics within the biotech or pharmaceutical industry, with a focus on oncology and/or CNS.
- Proven track record of leading statistical aspects of clinical trials from design to regulatory submission.
- Strong knowledge of statistical software (e.g., SAS, R) and clinical trial databases.
- Excellent communication and interpersonal skills, with the ability to work effectively in a collaborative team environment.
- Detail-oriented with strong problem-solving skills and the ability to manage multiple projects simultaneously.
Why Join Us:
- Be part of a passionate team dedicated to making a difference in patients' lives.
- Opportunity to work on innovative therapies in oncology and CNS.
- Competitive salary and benefits package.
- Collaborative and supportive work environment