Joulé
Temp - Biostatistician - Early Clinical Development
Job Location
Sleepy Hollow, NY, United States
Job Description
Job title: Biostatistician - Early Clinical Development
Location: Fully Remote
Pay Rate: $60/hr - $70/hr - Depending on level of experience
Contract
Excellent contract opportunity with a global pharmaceutical company. Must have a MS or PhD in Statistics/Biostatistics with 2+ years early phase clinical trial experience. The Biostatistician implements and executes methodological and statistical aspects of clinical studies under the
supervision of Therapeutic Area lead biostatistician or project lead statistician. In some cases, principal function
could be to develop/employ technical expertise in a particular statistical area or application.
In this role, a typical day might include:
Under direct supervision and guidance of senior departmental staff, provide support to a clinical study team on all relevant statistical matters.
As member of study team, ensure the clinical study is conducted in a manner that supports planned statistical analysis.
Under supervision and guidance of senior departmental staff, participate in preparation of study protocol and amendments.
???????Perform relevant sample size calculations and write statistical methodology section of the protocol.
This role might be for you if can:
Review case report form (CRF) and provide comments and feedback.
Develop statistical analysis plan (SAP).
Provide programming team with definitions and documentation for derived variables needed to produce planned Tables, Figures and Listings (TFLs). Develop data and programming specifications jointly with programmers.
Perform statistical analysis according to the SAP, validate analysis programs, review TFLs, prepare statistical methods and results sections for the clinical study report (CSR), provide statistical insight into interpretation and discussion of study results, and work with the study team to move the CSR through review /approval process.
Support/participate in project related activities including preparation of BLA submissions and oversee CRO deliverables for studies contracted out
To be considered for this opportunity, you must have the following:
Master Degree in related field required
2+ years of relevant experience
Location: Sleepy Hollow, NY, US
Posted Date: 11/28/2024
Location: Fully Remote
Pay Rate: $60/hr - $70/hr - Depending on level of experience
Contract
Excellent contract opportunity with a global pharmaceutical company. Must have a MS or PhD in Statistics/Biostatistics with 2+ years early phase clinical trial experience. The Biostatistician implements and executes methodological and statistical aspects of clinical studies under the
supervision of Therapeutic Area lead biostatistician or project lead statistician. In some cases, principal function
could be to develop/employ technical expertise in a particular statistical area or application.
In this role, a typical day might include:
Under direct supervision and guidance of senior departmental staff, provide support to a clinical study team on all relevant statistical matters.
As member of study team, ensure the clinical study is conducted in a manner that supports planned statistical analysis.
Under supervision and guidance of senior departmental staff, participate in preparation of study protocol and amendments.
???????Perform relevant sample size calculations and write statistical methodology section of the protocol.
This role might be for you if can:
Review case report form (CRF) and provide comments and feedback.
Develop statistical analysis plan (SAP).
Provide programming team with definitions and documentation for derived variables needed to produce planned Tables, Figures and Listings (TFLs). Develop data and programming specifications jointly with programmers.
Perform statistical analysis according to the SAP, validate analysis programs, review TFLs, prepare statistical methods and results sections for the clinical study report (CSR), provide statistical insight into interpretation and discussion of study results, and work with the study team to move the CSR through review /approval process.
Support/participate in project related activities including preparation of BLA submissions and oversee CRO deliverables for studies contracted out
To be considered for this opportunity, you must have the following:
Master Degree in related field required
2+ years of relevant experience
Location: Sleepy Hollow, NY, US
Posted Date: 11/28/2024
Contact Information
| Contact | Human Resources Joulé |
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