*Note: Position is not with our direct client.*
Dear Partners:-
Please find the requirement currently open.
*
Statistician Consultant
*
*
Stamford, CT
12 months
Open
*
*They have to have Phase I exp. and a min. of 2-3 years exp. In Pharma or
CRO.*
• Statistical design and analysis of Phase 1 studies
• Communicate with CRO statisticians in planning and reviewing Phase 1
statistical analysis
• Interact closely with Clinical Pharmacology colleagues in order to meet
tight project deliverablesCollaborates and interacts with the
clinical/medical staff utilizing technical knowledge and experience in the
design, development, analysis, and reporting of Phase I clinical studies
• Provides input into protocol development and review
• Prepares analytical plans and conducts statistical analysis of Phase 1
clinical data using appropriate statistical models and methods
• Works with CRO statistical colleagues in planning the programming
necessary to effectively analyze, summarize, and display data from Phase 1
clinical studies Review CRO provided statistical deliverables of 2 Butrans
bioequivalence studies
• Review and comment on draft TLGs and analysis data sets
• Review clinical study reports for statistical accuracy
• Assist in the design of at least 2 HYD Phase 1 studies. Develop the
statistical sections of these protocols.
• Review CRO provided statistical deliverables of ONU abuse liability
studies. Review and comment on draft TLGs and analysis data sets. Review
clinical study reports for statistical accuracy.
• Provide statistical consultation to Clinical Pharmacology staff, as
needed.
• Statistical Consultant candidate must be experienced in Phase 1 studies.
Critical deliverables for the Statistical
*
*
Please respond with *Resume, Rate, Current Location and Phone numbers of the
Consultant*. Make sure the Consultant's skills match the requirement.
I will contact you, if I need more information.
*
*
*Regards,*
*
*
*Palak Patel*
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**.*
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