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Form of workJob Description
Position Details:
Our client, a world-leading Pharmaceutical Company in Collegeville, PA is currently looking for a Statistical Analyst to join their expanding team.
Job Title: Statistical Analyst / SAS / Clinical Trials
Duration: 12 months contract, extendable up to 36 months
Location: Collegeville, PA
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:
Statistical Analyst
Summary:
The Statistical Analyst will assist asset/study statisticians to fulfill the analytical requests using multiple data sources to answer questions related to clinical trials and epidemiological research on vaccine development in pharmaceutical settings.
The analyst will use statistical software to analyze, summarize and report data.
This person will also perform analysis with clinical trial or research data to provide support to publications and method development. Will deliver technical presentations as required.
The objective is to provide quantitative support in analyzing clinical trials/epidemiology study/healthcare data.
The responsibilities may include contributing to assisting statisticians in developing study protocols and statistical analysis plans, and working with other lines of clinical/medicine/scientific team, to execute the statistical analysis plan.
This candidate will need to work under the Pharma regulation setting to make sure the work is conducted with high quality and in compliance.
Responsibilities:
Assist in developing statistical analysis plan (SAP) and analysis table/listing/figure (TLF)
Write analytical programs to generate analysis TLFs, and/or independently validate/QC existing TLFs using SAS statistical software
Prepare standardized analytical SAS data set by industry standard from varied data source with varied format, may need to clarify the data inconsistency with sites/collaborators
Perform quality control checks for programming work and keep good documentation
Understand data structure and analyze datasets from variate source to answer research questions
Communicate with the study team to understand the research need and to report data.
Qualifications:
Master's degree in statistics or related subjects required (PhD or MD acceptable)
A minimum of 2+ years of pharmaceutical/CRO experience analyzing life science data
Strong statistical analysis skills
Good understanding of statistical methods and interpretation of statistical outputs
Proficiency in SAS and Excel is required
Experience with other statistical packages such as R, is preferred
Proficiency in several statistical software packages, especially good skills in SAS programming
Database management skills
Experience with medical terminology and understanding of clinical/epidemiology research is preferred
Experience with visualization software is beneficial
Good oral and written communication skills
Work within a team environment to ensure alignment of common goals and maintain positive interaction with team members and internal peers
Work independently on multiple projects prioritizing according to project needs.
Location:
This is a fully onsite position located in Collegeville, PA
Our client, a world-leading Pharmaceutical Company in Collegeville, PA is currently looking for a Statistical Analyst to join their expanding team.
Job Title: Statistical Analyst / SAS / Clinical Trials
Duration: 12 months contract, extendable up to 36 months
Location: Collegeville, PA
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:
Statistical Analyst
Summary:
The Statistical Analyst will assist asset/study statisticians to fulfill the analytical requests using multiple data sources to answer questions related to clinical trials and epidemiological research on vaccine development in pharmaceutical settings.
The analyst will use statistical software to analyze, summarize and report data.
This person will also perform analysis with clinical trial or research data to provide support to publications and method development. Will deliver technical presentations as required.
The objective is to provide quantitative support in analyzing clinical trials/epidemiology study/healthcare data.
The responsibilities may include contributing to assisting statisticians in developing study protocols and statistical analysis plans, and working with other lines of clinical/medicine/scientific team, to execute the statistical analysis plan.
This candidate will need to work under the Pharma regulation setting to make sure the work is conducted with high quality and in compliance.
Responsibilities:
Assist in developing statistical analysis plan (SAP) and analysis table/listing/figure (TLF)
Write analytical programs to generate analysis TLFs, and/or independently validate/QC existing TLFs using SAS statistical software
Prepare standardized analytical SAS data set by industry standard from varied data source with varied format, may need to clarify the data inconsistency with sites/collaborators
Perform quality control checks for programming work and keep good documentation
Understand data structure and analyze datasets from variate source to answer research questions
Communicate with the study team to understand the research need and to report data.
Qualifications:
Master's degree in statistics or related subjects required (PhD or MD acceptable)
A minimum of 2+ years of pharmaceutical/CRO experience analyzing life science data
Strong statistical analysis skills
Good understanding of statistical methods and interpretation of statistical outputs
Proficiency in SAS and Excel is required
Experience with other statistical packages such as R, is preferred
Proficiency in several statistical software packages, especially good skills in SAS programming
Database management skills
Experience with medical terminology and understanding of clinical/epidemiology research is preferred
Experience with visualization software is beneficial
Good oral and written communication skills
Work within a team environment to ensure alignment of common goals and maintain positive interaction with team members and internal peers
Work independently on multiple projects prioritizing according to project needs.
Location:
This is a fully onsite position located in Collegeville, PA
