Note: The job is a remote job and is open to candidates in USA. Sunrise Systems, Inc. is seeking a Biostatistics Consultant to support statistical deliverables for a client's oncology program. The consultant will lead and validate clinical-trial analyses, review datasets and data standards, generate tables, figures, and listings, interpret results, and contribute statistical content for publications while collaborating with cross-functional teams.
Responsibilities
- Lead Statistical Efforts: Serve as the primary biostatistician for a study within a project team, supporting closeout activities and reviewing, validating, and executing analyses
- Provide Technical Guidance: Offer guidance to statistical programmers on developing SDTM/ADaM datasets and TLFs (Tables, Listings, and Figures) specifications, as well as perform quality checks on statistical programming efforts as needed
- Communication Skills: Strong written and verbal communication skills with the ability to present complex statistical concepts to both technical and non-technical audiences
- Collaboration: Proven ability to work effectively as part of a cross-functional team
- Problem-Solving: Strong analytical and problem-solving skills with the ability to make strategic decisions based on data-driven insights
- Statistical Expertise: In-depth knowledge of statistical methods and their application in oncology clinical trials
- Software Proficiency: Proficient in statistical programming languages and software, such as SAS and R, with the ability to guide data analysis and interpretation
- Data Standards: Experience with data standards such as CDISC SDTM and ADaM, including overseeing the development and quality control of specifications
- Quality Control: Strong attention to detail and commitment to ensuring the accuracy and integrity of statistical analyses and programming outputs
Skills
- * Communication Skills: Strong written and verbal communication skills with the ability to present complex statistical concepts to both technical and non-technical audiences
- * Collaboration: Proven ability to work effectively as part of a cross-functional team
- * Problem-Solving: Strong analytical and problem-solving skills with the ability to make strategic decisions based on data-driven insights
- * Statistical Expertise: In-depth knowledge of statistical methods and their application in oncology clinical trials
- * Software Proficiency: Proficient in statistical programming languages and software, such as SAS and R, with the ability to guide data analysis and interpretation
- * Data Standards: Experience with data standards such as CDISC SDTM and ADaM, including overseeing the development and quality control of specifications
- * Quality Control: Strong attention to detail and commitment to ensuring the accuracy and integrity of statistical analyses and programming outputs
- * PhD or MS in statistics or biostatistics
- * Broad and thorough understanding of statistical principles, up-to-date statistical design and methodologies, and their applications into clinical trial
- * Effective writing and communication skills: able to explain to team clearly and help team understand complex statistical design, methodology, decision rule, analysis plan and statistical report
- * Experience with Bayesian modeling and Analysis
- * Experienced with SAS programming, R programming and other statistical software
- * Ideal 3-year (for PhD) or 5-year (for MS) with experience in clinical trials
Benefits
- ACA compliant medical coverage
- Dental insurance
- Vision insurance
- Sick time benefits as required per State regulations
Company Overview
Company H1B Sponsorship