What are the responsibilities and job description for the Statistical Programmer position at CGXP Consulting LLC?
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.
Requirements:
- 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 studies
- Pharmaceutical, CRO, or related industry experience with clinical trials, including interaction with Regulatory Agencies, especially FDA.
Job Type: Contract
Experience level:
- 4 years
Schedule:
- Day shift
- Monday to Friday
Work Location: In person
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