Join to apply for the Senior Biostatistician role at Cardiovascular Research Foundation Join to apply for the Senior Biostatistician role at Cardiovascular Research Foundation Cardiovascular Research Foundation provided pay range This range is provided by Cardiovascular Research Foundation. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $105,000.00/yr - $115,000.00/yr This role is subject to a flexible hybrid work arrangement requiring a minimum of 1-2 pre-determined days per week in our mid-town office. Summary As a member of clinical trial teams, the Senior Statistician brings statistical expertise to the design, conduct, analysis and reporting of clinical studies, in the pre-clinical, Phases I to IV, and post-marketing, stages of study. The Senior Statistician works as a member of cross-functional teams and continuously strives to ensure timely delivery and scientific validity of results. He/she will work closely with statistical team and company programmers to ensure a seamless, accurate and timely delivery of scientific data reporting of study trials and activities sponsored or conducted by company. The Senior Biostatistician supports physicians/ principal investigators in all academic/ sponsor-driven quantitative analysis which includes: Producing statistical analysis plans, creating table-shells, contributing to written manuscripts and research articles, and participating on clinical safety boards. In addition, we expect a high level of creative statistical thinking and theoretical knowledge from the Senior Biostatistician. Essential Duties And Responsibilities Design, analyze, and report on new/continuing sponsor-related clinical trials Review and prepare statistical sections of study protocols and perform sample size calculations Review and prepare detailed statistical analysis plans and table/listing/graph shells Work with a multifunctional team of SAS programmers, data managers, and physicians in reviewing case report forms, identifying data quality issues, and producing analysis datasets and data outputs Validate statistical analyses to ensure data accuracy in final clinical study reports and provide statistical interpretations of results Interface with project management, functional team members and investigators to ensure a timely, precise and accurate clinical data reporting process Interact with medical directors/writers to ensure appropriateness of data inferences; draft pertinent sections of a clinical trial report or statistical report Use SAS software (knowledge of more programming languages desired) Collaborate with Cardiovascular Physicians on academic research Participate in Data Safety Monitoring Boards Represent the Biostatistics group in regulatory agency and project team meetings Qualifications Possess a PhD degree in Biostatistics or Statistics, preferably experience in clinical trials Application experience in cardiology and/or prior experience in medical device clinical trials is a plus Proficiency in SAS programming Experience in authoring manuscripts, clinical documents and templates Structure research hypotheses with sound analysis Understand the clinical trial process, and the statistician’s role. Benefits Choice of health plans include medical, Dental, and vision coverage Company-paid short-term and long-term disability and life insurance Health and dependent care flexible spending accounts Pre-tax travel expenses through TransitChek program 401(k) plan Generous paid time off (PTO) Ten paid holidays each year Compensation The hiring range for this position is $105,000 - $115,000 per year. The annual salary that will ultimately be offered to the successful candidate will depend on job-related knowledge, education, skills, and experience.
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