Aequor
Statistical Analyst
Aequor, Collegeville, Pennsylvania, United States, 19426
Job Description:
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 setting. 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.
Job ObjectivesThe objective is to provide quantitative support in analyzing clinical trials/epidemiology study/healthcare data. The responsibilities may include contributing to assist statistician to develop study protocols and statistical analysis plans, 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.
Key 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
At least Master's degree in statistics or related subjects. (PhD or MD acceptable)
At least 2 years of pharmaceutical/CRO experience analyzing life science data.
Strong statistical analysis skills.
Good understanding in statistical methods and interpretation of statistical outputs.
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 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.
Software Literacy
Proficiency in SAS and Excel is required.
Experience with other statistical packages such as R is preferred.
Required Skills
SAS
Excel
2 years of pharmaceutical/CRO experience analyzing life science data.
Preferred Skills
Other statistical packages such as R
Medical Terminology
Understanding of Clinical/Epidemiology Research
Visualization Software
Interview Process1st Phone or Teams Interview or Panel Teams Interview with potential 2nd Interview. 100% Onsite (Collegeville preferred, local to *** location (EST/CST Zone preferred)).
#J-18808-Ljbffr
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 setting. 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.
Job ObjectivesThe objective is to provide quantitative support in analyzing clinical trials/epidemiology study/healthcare data. The responsibilities may include contributing to assist statistician to develop study protocols and statistical analysis plans, 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.
Key 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
At least Master's degree in statistics or related subjects. (PhD or MD acceptable)
At least 2 years of pharmaceutical/CRO experience analyzing life science data.
Strong statistical analysis skills.
Good understanding in statistical methods and interpretation of statistical outputs.
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 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.
Software Literacy
Proficiency in SAS and Excel is required.
Experience with other statistical packages such as R is preferred.
Required Skills
SAS
Excel
2 years of pharmaceutical/CRO experience analyzing life science data.
Preferred Skills
Other statistical packages such as R
Medical Terminology
Understanding of Clinical/Epidemiology Research
Visualization Software
Interview Process1st Phone or Teams Interview or Panel Teams Interview with potential 2nd Interview. 100% Onsite (Collegeville preferred, local to *** location (EST/CST Zone preferred)).
#J-18808-Ljbffr