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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 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 Objectives:
The 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:
1. Assist in developing statistical analysis plan (SAP) and analysis table/listing/figure (TLF).
2. Write analytical programs to generate analysis TLFs, and/or independently validate/QC existing TLFs using SAS statistical software.
3. Prepare standardized analytical SAS data set by industry standard from varied data source with varied format, may need to clarify the data inconsistence with sites/collaborators.
4. Perform quality control checks for programming work and keep good documentation.
5. Understand data structure and analyze datasets from variate source to answer research questions.
6. Communicate with the study team to understand the research need and to report data.
Qualifications:
1. At least Master's degree in statistics or related subjects. (PhD or MD acceptable)
2. At least 2 years of pharmaceutical/CRO experience analyzing life science data.
3. Strong statistical analysis skills.
4. Good understanding in statistical methods and interpretation of statistical outputs.
5. Proficiency in several statistical software packages, especially good skills in SAS programming.
6. Database management skills.
7. Experience with medical terminology and understanding of clinical/epidemiology research is preferred.
8. Experience with visualization software is beneficial.
9. Good oral and written communication skills.
10. Work within team environment to ensure alignment of common goals and maintain positive interaction with team members and internal peers.
11. Work independently on multiple projects prioritizing according to project needs.
Software Literacy:
1. Proficiency in SAS and Excel is required.
2. Experience with other statistical packages such as R, is preferred.
Required Skills:
1. SAS
2. Excel
3. 2 years of pharmaceutical/CRO experience analyzing life science data.
Preferred Skills:
1. Other statistical packages such as R
2. Medical Terminology
3. Understanding of Clinical/Epidemiology Research
4. Visualization Software
Interview Process:
1st Phone or Teams Interview or Panel Teams Interview
with potential 2nd Interview
100% Onsite (Collegeville preferred, local to Pharmaceutical location (EST/CST Zone preferred))
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 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 Objectives:
The 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:
1. Assist in developing statistical analysis plan (SAP) and analysis table/listing/figure (TLF).
2. Write analytical programs to generate analysis TLFs, and/or independently validate/QC existing TLFs using SAS statistical software.
3. Prepare standardized analytical SAS data set by industry standard from varied data source with varied format, may need to clarify the data inconsistence with sites/collaborators.
4. Perform quality control checks for programming work and keep good documentation.
5. Understand data structure and analyze datasets from variate source to answer research questions.
6. Communicate with the study team to understand the research need and to report data.
Qualifications:
1. At least Master's degree in statistics or related subjects. (PhD or MD acceptable)
2. At least 2 years of pharmaceutical/CRO experience analyzing life science data.
3. Strong statistical analysis skills.
4. Good understanding in statistical methods and interpretation of statistical outputs.
5. Proficiency in several statistical software packages, especially good skills in SAS programming.
6. Database management skills.
7. Experience with medical terminology and understanding of clinical/epidemiology research is preferred.
8. Experience with visualization software is beneficial.
9. Good oral and written communication skills.
10. Work within team environment to ensure alignment of common goals and maintain positive interaction with team members and internal peers.
11. Work independently on multiple projects prioritizing according to project needs.
Software Literacy:
1. Proficiency in SAS and Excel is required.
2. Experience with other statistical packages such as R, is preferred.
Required Skills:
1. SAS
2. Excel
3. 2 years of pharmaceutical/CRO experience analyzing life science data.
Preferred Skills:
1. Other statistical packages such as R
2. Medical Terminology
3. Understanding of Clinical/Epidemiology Research
4. Visualization Software
Interview Process:
1st Phone or Teams Interview or Panel Teams Interview
with potential 2nd Interview
100% Onsite (Collegeville preferred, local to Pharmaceutical location (EST/CST Zone preferred))
