Katalyst Healthcares and Life Sciences
Statistical Programmer
Katalyst Healthcares and Life Sciences, Rahway, New Jersey, us, 07065
Responsibilities:
Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies.Provide statistical oversight to studies and assure adequate quality and consistency with project requirements.Responsible for assuring that data for statistical analyses are complete, accurate and consistent.Responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions.Responsible for validity of analysis and explore alternative analysis strategies as needed.Qualifications:
4+ years' experience preferred leading late phase studies.MS or PhD in Statistics, Biostatistics or related field. PhD with 3-5 years of experience or MS with 6-8 years of experience.Must have experience in Oncology & AdAM.Strong oral and written communications skills, with ability to effectively communicate internally and with clients.Infectious disease background + experience working on observational studiesPharmaceutical, CRO, or related industry experience with clinical trials, including interaction with Regulatory Agencies, especially FDA.
Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies.Provide statistical oversight to studies and assure adequate quality and consistency with project requirements.Responsible for assuring that data for statistical analyses are complete, accurate and consistent.Responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions.Responsible for validity of analysis and explore alternative analysis strategies as needed.Qualifications:
4+ years' experience preferred leading late phase studies.MS or PhD in Statistics, Biostatistics or related field. PhD with 3-5 years of experience or MS with 6-8 years of experience.Must have experience in Oncology & AdAM.Strong oral and written communications skills, with ability to effectively communicate internally and with clients.Infectious disease background + experience working on observational studiesPharmaceutical, CRO, or related industry experience with clinical trials, including interaction with Regulatory Agencies, especially FDA.