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Form of work Position Details:
Our client, a world-leading Pharmaceutical Company in Irvine, CA is currently looking for a Biostatistician / Clinical Trials / HYBRID SCHEDULE to join their expanding team.
Job Title: Biostatistician / Clinical Trials / HYBRID SCHEDULE
Duration: 12 months contract, extendable up to 24 Months
Location: Irvine, CA
Hybrid Schedule: Roughly 1-2 days in the office per week, the actual day varies from team to team, could be Tue. and Thu, or Mon and Wed.
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Hybrid Schedule: Roughly 1-2 days in the office per week, the actual day varies from team to team, could be Tue. and Thu, or Mon and Wed.
General Summary:
Supports in-house statistical and analytical services in support of clinical trials, regulatory approvals, marketing efforts, quality initiatives.
Duties & Responsibilities:
Edits and finalizes statistical analysis plans and system programming plans for all phases of clinical studies.
Supports complex activities of clinical study design related to implementing a clinic.
Conducts training sessions and ensures the preparation of presentation materials for statisticians and non-statisticians on statistical methods and tests.
Reports on the findings of statistical analyses and publications in preparation for new product applications to regulatory agencies.
Prepares and documents facts to enable management to write and support trial reports and publications.
Ensures that new and revised statistical standards, tests, and processes are implemented for increased accuracy and efficiency.
Oversees the maintenance of important information on data management, investigator initiated trials, and registries.
Resolves complex questions on statistical issues from the business units and external customers.
Work Experience:
Generally Requires 2-3 Years Work Experience Education Required: Masters Degree
Our client, a world-leading Pharmaceutical Company in Irvine, CA is currently looking for a Biostatistician / Clinical Trials / HYBRID SCHEDULE to join their expanding team.
Job Title: Biostatistician / Clinical Trials / HYBRID SCHEDULE
Duration: 12 months contract, extendable up to 24 Months
Location: Irvine, CA
Hybrid Schedule: Roughly 1-2 days in the office per week, the actual day varies from team to team, could be Tue. and Thu, or Mon and Wed.
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Hybrid Schedule: Roughly 1-2 days in the office per week, the actual day varies from team to team, could be Tue. and Thu, or Mon and Wed.
General Summary:
Supports in-house statistical and analytical services in support of clinical trials, regulatory approvals, marketing efforts, quality initiatives.
Duties & Responsibilities:
Edits and finalizes statistical analysis plans and system programming plans for all phases of clinical studies.
Supports complex activities of clinical study design related to implementing a clinic.
Conducts training sessions and ensures the preparation of presentation materials for statisticians and non-statisticians on statistical methods and tests.
Reports on the findings of statistical analyses and publications in preparation for new product applications to regulatory agencies.
Prepares and documents facts to enable management to write and support trial reports and publications.
Ensures that new and revised statistical standards, tests, and processes are implemented for increased accuracy and efficiency.
Oversees the maintenance of important information on data management, investigator initiated trials, and registries.
Resolves complex questions on statistical issues from the business units and external customers.
Work Experience:
Generally Requires 2-3 Years Work Experience Education Required: Masters Degree
