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Searching for Qualified Statisticians in PA, MA, IN and WI!!
I am in search of qualified Statisticians for several positions in Collegeville, PA, Cambridge, MA, Indianapolis, IN and Madison, WI. These are permanent positions through inVentiv Clinical Solutions, and come with excellent benefits and very competitive pay! I have included the job descriptions below for your review. If you are interested in hearing more details about these opportunities, please feel free to call or email me. I am in my office Monday through Friday 9:00am to 5:30pm EST. I look forward to hearing from you!
Statistician - Indianapolis, IN
JOB SUMMARY
Responsible for all statistical aspects (design, analysis and reporting) relating to clinical trial investigations and performing or validating statistical programming. Works in close collaboration with a Senior Statistician.
DUTIES AND RESPONSIBILITIES
Write statistical sections of study protocols in collaboration with the Senior Statistician.
Assist Senior Statistician with development of Statistical Analysis Plans (SAP).
Perform statistical analyses according to SAP in collaboration with the Senior Statistician.
Validate programs that create tables, figures, and listings according to SAP.
Responsible for final check of all key deliverables such as SAP, tables, listings figures.
Develop therapeutic area knowledge necessary to perform other essential functions.
Comply with all relevant laws, regulations, policies, and procedures.
EDUCATION, TRAINING AND PRIOR EXPERIENCE REQUIREMENTS Minimum of B.S. degree in statistics or biostatistics or equivalent experience to compensate degree. Must have knowledge of commonly used statistical concepts, practices, and procedures. Excellent oral and written communication skills are expected.
Madison, WI - Statistician
This team will work under the direction and guidance of a Sr. Director of Statistics and function on specific project work. Statisticians will travel to San Francisco to interact and capture the corporate culture of casual intensity and learn client SOPs. This is a two year plus commitment that will either transfer into permanent client employment or continual annual extensions.
Compensation is commensurate with experience and education.
Requirements:
PhD candidates with 1+ yrs clinical trials experience or MS candidates with 3+ years experience at a Pharma, CRO, or Biotech. and at least one year of clinical development experience, good SAS programming skills and strong communication skills. Looking for individuals with strong study report writing and NDA filing experience. Any filing or publication experience is a major plus. The T.A. will be Bio-therapeutics and Oncology.
Description:
Statistician will handle specific tasks across multiple projects. Provide statistical consulting regarding clinical trial implementation, including but not limited to drafting of protocols and providing feedback on CRF designs, SAP development, exploratory data analyses, study report writing, study design, read technical literature, manuscript preparation, simulation programming, etc.. Create analysis plans and TLG (tables, listings, and graphs) mock-ups. Provide statistical consulting regarding planning for a BLA filing.
Collegeville, PA and Cambridge, MA - Statistician
Major Global pharmaceutical company who discovers, develops, manufactures and markets innovative medicines that are leading the way to a healthier world is seeking a Biostatistician. You will be an important part of a leading research and manufacturing organization.
Responsibilities:
As a Biostatistician you will participate in the planning and reporting of clinical trials, including addressing study design, sample size, CRF design and proposed methods of analysis and associated liaisons with other clinical/operations staff. You will ensure the maintenance or productivity and adherence to project target dates with respect to clinical development plans, clinical analysis plans, protocol development, analysis and report preparation for assigned projects. You will have responsibility for the statistical analysis and interpretation of data and presentation of results in co-authored CSRs and will also have responsibility for the development and execution of validated SAS programs to list and summarize clinical trial data. You will also conduct peer review of project related work performed by other statisticians, maintain compliance with the latest Biostatistical regulatory requirements, maintain study and project documentation and files according to departmental policy, and maintain external academic, professional and industry contacts.
Additional:
The Biostatistics department provides statistical support to early drug development projects including discovery. As a Biostatistician, you are expected to be knowledgeable with statistical methods for dose response studies, assay development, and comparative in vivo experiments. You should have expertise in regression methods, analysis of variance, and mixed models, and experience with generalized linear models and survival models will useful. You will be responsible for statistical support for multiple discovery projects. You will consult with discovery on the experimental design, sample size, protocol development, data analysis, and data interpretation for their studies. You will also support activities that cross multiple projects such as methodological research, staff training programs, process improvement initiatives, and consultation with other staff members.
Education:
You must have a MS in statistics or in mathematics with a minimum of 5 years of clinical trials experience, or a Ph.D. or Doctorate, with a minimum of 1 year of relevant work experience. Familiarity with statistical software packages a plus.
Compensation/Benefits:
We offer competitive compensation and benefit programs including full medical and dental insurance coverage, holiday and vacation paid time off, business casual attire, 401K programs, Life Insurance, Long Term Disability and professional development programs.
Regards,
Josh
Josh Cooksey
Recruiter - Team Lead
inVentiv Clinical Solutions
1025 Greenwood Boulevard, Suite 100
Lake Mary, FL 32746
Toll Free Phone: (800) 684-9921 x203
Direct Local Phone: (407) 548-0653
Fax: 888-513-4285
Cell Phone: (352) 318-8906
JCooksey@inventivclinical.com
www.inventivclinical.com
..specializing in the placements of:
Clinical Data Managers
SAS Programmers
Statisticians
Monitors & CRAs
Study & Project Managers
Safety/Regulatory
Study Specialists
Medical Writers
Scientists/Lab Staff
all across the United States
Statistician - Indianapolis, IN
JOB SUMMARY
Responsible for all statistical aspects (design, analysis and reporting) relating to clinical trial investigations and performing or validating statistical programming. Works in close collaboration with a Senior Statistician.
DUTIES AND RESPONSIBILITIES
Write statistical sections of study protocols in collaboration with the Senior Statistician.
Assist Senior Statistician with development of Statistical Analysis Plans (SAP).
Perform statistical analyses according to SAP in collaboration with the Senior Statistician.
Validate programs that create tables, figures, and listings according to SAP.
Responsible for final check of all key deliverables such as SAP, tables, listings figures.
Develop therapeutic area knowledge necessary to perform other essential functions.
Comply with all relevant laws, regulations, policies, and procedures.
EDUCATION, TRAINING AND PRIOR EXPERIENCE REQUIREMENTS Minimum of B.S. degree in statistics or biostatistics or equivalent experience to compensate degree. Must have knowledge of commonly used statistical concepts, practices, and procedures. Excellent oral and written communication skills are expected.
Madison, WI - Statistician
This team will work under the direction and guidance of a Sr. Director of Statistics and function on specific project work. Statisticians will travel to San Francisco to interact and capture the corporate culture of casual intensity and learn client SOPs. This is a two year plus commitment that will either transfer into permanent client employment or continual annual extensions.
Compensation is commensurate with experience and education.
Requirements:
PhD candidates with 1+ yrs clinical trials experience or MS candidates with 3+ years experience at a Pharma, CRO, or Biotech. and at least one year of clinical development experience, good SAS programming skills and strong communication skills. Looking for individuals with strong study report writing and NDA filing experience. Any filing or publication experience is a major plus. The T.A. will be Bio-therapeutics and Oncology.
Description:
Statistician will handle specific tasks across multiple projects. Provide statistical consulting regarding clinical trial implementation, including but not limited to drafting of protocols and providing feedback on CRF designs, SAP development, exploratory data analyses, study report writing, study design, read technical literature, manuscript preparation, simulation programming, etc.. Create analysis plans and TLG (tables, listings, and graphs) mock-ups. Provide statistical consulting regarding planning for a BLA filing.
Collegeville, PA and Cambridge, MA - Statistician
Major Global pharmaceutical company who discovers, develops, manufactures and markets innovative medicines that are leading the way to a healthier world is seeking a Biostatistician. You will be an important part of a leading research and manufacturing organization.
Responsibilities:
As a Biostatistician you will participate in the planning and reporting of clinical trials, including addressing study design, sample size, CRF design and proposed methods of analysis and associated liaisons with other clinical/operations staff. You will ensure the maintenance or productivity and adherence to project target dates with respect to clinical development plans, clinical analysis plans, protocol development, analysis and report preparation for assigned projects. You will have responsibility for the statistical analysis and interpretation of data and presentation of results in co-authored CSRs and will also have responsibility for the development and execution of validated SAS programs to list and summarize clinical trial data. You will also conduct peer review of project related work performed by other statisticians, maintain compliance with the latest Biostatistical regulatory requirements, maintain study and project documentation and files according to departmental policy, and maintain external academic, professional and industry contacts.
Additional:
The Biostatistics department provides statistical support to early drug development projects including discovery. As a Biostatistician, you are expected to be knowledgeable with statistical methods for dose response studies, assay development, and comparative in vivo experiments. You should have expertise in regression methods, analysis of variance, and mixed models, and experience with generalized linear models and survival models will useful. You will be responsible for statistical support for multiple discovery projects. You will consult with discovery on the experimental design, sample size, protocol development, data analysis, and data interpretation for their studies. You will also support activities that cross multiple projects such as methodological research, staff training programs, process improvement initiatives, and consultation with other staff members.
Education:
You must have a MS in statistics or in mathematics with a minimum of 5 years of clinical trials experience, or a Ph.D. or Doctorate, with a minimum of 1 year of relevant work experience. Familiarity with statistical software packages a plus.
Compensation/Benefits:
We offer competitive compensation and benefit programs including full medical and dental insurance coverage, holiday and vacation paid time off, business casual attire, 401K programs, Life Insurance, Long Term Disability and professional development programs.
Regards,
Josh
Josh Cooksey
Recruiter - Team Lead
inVentiv Clinical Solutions
1025 Greenwood Boulevard, Suite 100
Lake Mary, FL 32746
Toll Free Phone: (800) 684-9921 x203
Direct Local Phone: (407) 548-0653
Fax: 888-513-4285
Cell Phone: (352) 318-8906
JCooksey@inventivclinical.com
www.inventivclinical.com
..specializing in the placements of:
Clinical Data Managers
SAS Programmers
Statisticians
Monitors & CRAs
Study & Project Managers
Safety/Regulatory
Study Specialists
Medical Writers
Scientists/Lab Staff
all across the United States
Views: 7
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Permalink Reply by Jacqueline Shaffer on -
I have a Master's degree in Statistics and am interested in working as a Statistician.
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