Join a leading healthcare organization as a Senior Biostatistician. Contribute to impactful clinical trials and regulatory submissions. Work remotely and collaborate with dynamic cross-functional teams.
Senior Biostatistician
in Healthcare + Life Sciences ContractJob Detail
Job Description
Overview
- Join a dynamic team as a Senior Biostatistician, contributing statistical expertise to clinical trials and development plans for innovative healthcare solutions.
- Collaborate with cross-disciplinary teams to deliver statistical analyses and support regulatory submissions for clinical programs.
- Work remotely, leveraging advanced statistical methodologies to enhance clinical trial designs and outcomes.
- Engage in a fast-paced environment, applying biostatistical knowledge to impactful healthcare projects.
- Contribute to the statistical deliverables of clinical trials, ensuring compliance with regulatory standards.
- Utilize statistical software tools such as SAS and R to perform complex data analyses.
- Participate in the development of statistical models and innovative design approaches for clinical studies.
- Collaborate with stakeholders to communicate statistical findings and insights effectively.
Key Responsibilities & Duties
- Design and analyze clinical trials, contributing to the statistical aspects of development plans.
- Collaborate with program partners to deliver statistical deliverables and support regulatory submissions.
- Ensure statistical processes align with company guidelines and regulatory requirements.
- Develop and implement statistical models and methodologies for clinical studies.
- Provide expertise in drug development, applying biostatistical knowledge to clinical trials.
- Utilize statistical software tools to perform data analysis and generate insights.
- Lead and supervise statistical processes for multiple clinical trials.
- Communicate complex statistical concepts effectively to stakeholders and team members.
Job Requirements
- Master's or Ph.D. in Statistics or related field with 5+ years of experience.
- Proficiency in statistical software such as SAS and R.
- Expertise in drug development and biostatistics application to clinical trials.
- Experience in regulatory submissions and statistical deliverables.
- Knowledge of eCRT, Define, and advanced statistical models.
- Ability to work autonomously and collaboratively within cross-disciplinary teams.
- Strong communication skills to explain complex statistical concepts.
- Preferred experience in therapeutic areas such as Immunology.
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