Biostatistician (full time or part-time) Entry/Mid/Senior/Principle
Inventiv Matrix is a Contract Research Organization company providing Data Management, Biostatistics and SAS Programming services for pharmaceutical/biotech companies. We are growing now and need some Biostatistician from different levels to join us.
The biostatistician providing statistical support of data analysis for data collected from clinical trials.
Job Responsibilities:
• Assists in writing statistical analysis plans and system programming plans for all phases of clinical studies.
• Supports the basic activities of clinical study design related to the implementation of a clinic.
• Coordinates training schedules and presentation materials for the training of statisticians and non-statisticians on statistical methods and tests.
• Formats reports on the findings of statistical analyses and publications in preparation for new product applications to regulatory agencies.
• Assists senior staff with the preparation and documentation of facts to write and support trial reports and publications
• Supports the implementation of new and revised statistical standards, tests, and processes for increased accuracy and efficiency.
• Coordinates documents and findings of revised changes to submission to management.
• Routes questions to senior biostatistics staff on statistical issues from the business units and external customersQualification:
Minimum education required for competent performance:
• Master Degree of statistics or related area, OR PHD degree preferred
Minimum experience (number of month/years and type of work experience beyond formal education) required for competent performance
Location:
• Bridgewater, NJ or St Louis, MO or Remote
Benefits:
• 401(k)
• Flexible schedule
• Paid time off
• Professional development assistance
• Tuition reimbursement
Compensation Package:
• Bonus opportunities
Schedule:
• Day shift
Education:
• Master's (Required)
Experience:
• Biostatistics: 1 year (Preferred)
• SAS: 2 years (Preferred)
Work Location: Remote
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The biostatistician providing statistical support of data analysis for data collected from clinical trials.
Job Responsibilities:
• Assists in writing statistical analysis plans and system programming plans for all phases of clinical studies.
• Supports the basic activities of clinical study design related to the implementation of a clinic.
• Coordinates training schedules and presentation materials for the training of statisticians and non-statisticians on statistical methods and tests.
• Formats reports on the findings of statistical analyses and publications in preparation for new product applications to regulatory agencies.
• Assists senior staff with the preparation and documentation of facts to write and support trial reports and publications
• Supports the implementation of new and revised statistical standards, tests, and processes for increased accuracy and efficiency.
• Coordinates documents and findings of revised changes to submission to management.
• Routes questions to senior biostatistics staff on statistical issues from the business units and external customersQualification:
Minimum education required for competent performance:
• Master Degree of statistics or related area, OR PHD degree preferred
Minimum experience (number of month/years and type of work experience beyond formal education) required for competent performance
Location:
• Bridgewater, NJ or St Louis, MO or Remote
Benefits:
• 401(k)
• Flexible schedule
• Paid time off
• Professional development assistance
• Tuition reimbursement
Compensation Package:
• Bonus opportunities
Schedule:
• Day shift
Education:
• Master's (Required)
Experience:
• Biostatistics: 1 year (Preferred)
• SAS: 2 years (Preferred)
Work Location: Remote
Apply tot his job
Apply To this Job