Job Description
We have a current opportunity for an AD Biostatistics on a permanent basis with an innovative oncology pharmaceutical company. This full time permanent position will be based in Jersey City, NJ (3x a week). For further information about this position please apply.
Salary: $180,000-210,000, 20% bonus + additional benefits
The AD Biostatistics - Oncology will provide statistical support for late-phase clinical trials within the Oncology Therapeutic Area. This role is crucial for the timely delivery of statistical deliverables and contributes significantly to the company's mission of advancing transformative therapies.
Key Responsibilities:
- Clinical Trial Design: Design clinical trials, provide strategic inputs, and innovative solutions to support data-driven quantitative decisions.
- Statistical Analysis: Conduct advanced statistical analysis ensuring robust and accurate data interpretation.
- Innovative Methods: Support the adoption of novel designs and innovative statistical methods.
- Collaboration: Facilitate execution and delivery by collaborating with cross-functional teams to achieve project objectives.
- Leadership: Lead and be accountable for study-level delivery strategies, including effective risk identification and mitigation.
Skills and Qualifications:
- Educational Background: Ph.D. or Master's degree in Biostatistics, Statistics, or a related field.
- Experience: Minimum of 6 years of experience in biostatistics, with at least 3 years in oncology clinical trials.
- Technical Expertise: Extensive knowledge of drug development, clinical study design, trial simulations, analysis methodology, and data interpretation.
- Regulatory Knowledge: Familiarity with FDA and ICH regulations and industry standards applicable to study design, data analysis, and regulatory submissions.
- Leadership: Proven ability to provide statistical leadership and support for quantitative decision-making, regulatory meetings, and submissions.
- Collaboration: Strong collaborative skills and ability to work effectively with cross-functional teams.
Preferred Qualifications:
- Experience with late stage oncology trials
- Submissions/regulatory experience
- Innovative thinker with a track record of driving the adoption of novel designs and complex modeling.
- Excellent communication skills, both written and verbal.
Benefits:
- Competitive salary and performance-based bonuses.
- Comprehensive health, dental, and vision insurance.
- Retirement savings plan with company match.
- Professional development opportunities.
- Flexible work arrangements.
Job Tags
Permanent employment, Full time, Flexible hours,