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Sr. Principal Statistician/Scientific Fellow

Location
Boston, MA

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Job Description:
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s Privacy Notice
, Privacy Policy
and Terms of Use
Job Description
Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a Sr. Principal Statistician/Scientific Fellow in our Cambridge office.
Here, everyone matters and you will be a vital contributor to our inspiring, bold mission.  As a Sr Statistician working on the Oncology team, you will be empowered to shape the contribution to Takeda's R&D vision, and a typical day will include: 
OBJECTIVE:
The purpose of this position is to provide study level statistical expertise by:
Participating in designing and independently analyzing and interpreting data from clinical studies.
Using standards to maximize global data integratability and interpretability.
Leveraging internal and external resources to achieve quality, timely and cost-effective study deliverables.
ACCOUNTABILITIES:
Represent the statistics function in support of clinical studies, generally supporting multiple studies at a time.
Provide statistical input to feasibility assessments, development and submission plans, and in support of regulatory submissions.
Provide statistical support with minimal supervision in the development and review of the study synopsis, protocol, statistical analysis plan, clinical study report, and other regulatory submission documents, ensuring accurate and statistically valid deliverables.
Implement project level database (including derived database), analysis and reporting standards. Provide suggestions to achieve high quality databases and specifications by working with Data Management and Programming at project level.
Plan and direct study-level analysis and reporting activities (eg, tables, listings, graphs) including review of work by programmers.
Identify study-level vendor requirements and participate in the evaluation/selection of analytical vendors. Provide technical oversight of statistical activities of external vendors to ensure timeliness and quality of analysis data and statistical outputs. Review and approve key statistical vendor deliverables.
Anticipate and communicate study level resource and quality issues that may impact deliverables or timelines.  Propose and implement solutions. Escalate issues to management as appropriate.
Consider and evaluate alternative analysis methodology and data presentation techniques. 
Support development and implementation of departmental standards and process improvements.
EDUCATION, EXPERIENCE AND SKILLS: 
PhD in statistics or biostatistics or equivalent with minimum of 1 year of relevant experience (including internships and statistical researches) or MS in statistics or biostatistics or equivalent with minimum of 3 years of relevant experience.
Good knowledge of clinical study designs, common analysis methods, descriptive and inferential statistics, summarization of data and presentation practices.
Good knowledge of the pharmaceutical industry including understanding of clinical drug development process and associated documents.
Knowledge of FDA and ICH regulations and industry standards applicable to the design and analysis of clinical trials.
Good knowledge of statistical programming languages (including SAS), software. Working knowledge of UNIX operating systems, and common software products and technologies used in conjunction with SAS (e.g., Microsoft OfficeÒ products).
General project management skills.
Good oral and written communications skills.
Good collaborative skills and ability to work with a cross-functional team.
WHAT TAKEDA CAN OFFER YOU:
401(k) with company match and Annual Retirement Contribution Plan
Tuition reimbursement
Company match of charitable contributions
Health & Wellness programs including onsite flu shots and health screenings
Generous time off for vacation and the option to purchase additional vacation days
Community Outreach Programs
Empowering Our People to Shine
Learn more at  takedajobs.com
Takeda is an EEO employer of minorities, women, disabled, protected veterans, and considers qualified applicants with criminal histories in accordance with applicable laws. For more information, visit  ****No Phone Calls or Recruiters Please.
*LI-KL1
Locations
Boston, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Apply Now
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence
and that I agree with
Takeda’s
Privacy Notice
, Privacy Policy and Terms of Use .
Job Description
Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a
 Sr. Principal Statistician/Scientific Fellow 
in our Cambridge office. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission.  As a
 Sr Statistician working on the Oncology
team, you will be empowered to shape the contribution to Takeda's R&D vision, and a typical day will include:  OBJECTIVE: The purpose of this position is to provide study level statistical expertise by: Participating in designing and independently analyzing and interpreting data from clinical studies.
Using standards to maximize global data integratability and interpretability.
Leveraging internal and external resources to achieve quality, timely and cost-effective study deliverables.
ACCOUNTABILITIES: Represent the statistics function in support of clinical studies, generally supporting multiple studies at a time.
Provide statistical input to feasibility assessments, development and submission plans, and in support of regulatory submissions.
Provide statistical support with minimal supervision in the development and review of the study synopsis, protocol, statistical analysis plan, clinical study report, and other regulatory submission documents, ensuring accurate and statistically valid deliverables.
Implement project level database (including derived database), analysis and reporting standards. Provide suggestions to achieve high quality databases and specifications by working with Data Management and Programming at project level.
Plan and direct study-level analysis and reporting activities (eg, tables, listings, graphs) including review of work by programmers.
Identify study-level vendor requirements and participate in the evaluation/selection of analytical vendors. Provide technical oversight of statistical activities of external vendors to ensure timeliness and quality of analysis data and statistical outputs. Review and approve key statistical vendor deliverables.
Anticipate and communicate study level resource and quality issues that may impact deliverables or timelines.  Propose and implement solutions. Escalate issues to management as appropriate.
Consider and evaluate alternative analysis methodology and data presentation techniques. 
Support development and implementation of departmental standards and process improvements.
EDUCATION, EXPERIENCE AND SKILLS:  PhD in statistics or biostatistics or equivalent with minimum of 1 year of relevant experience (including internships and statistical researches) or MS in statistics or biostatistics or equivalent with minimum of 3 years of relevant experience.
Good knowledge of clinical study designs, common analysis methods, descriptive and inferential statistics, summarization of data and presentation practices.
Good knowledge of the pharmaceutical industry including understanding of clinical drug development process and associated documents.
Knowledge of FDA and ICH regulations and industry standards applicable to the design and analysis of clinical trials.
Good knowledge of statistical programming languages (including SAS), software. Working knowledge of UNIX operating systems, and common software products and technologies used in conjunction with SAS (e.g., Microsoft OfficeÒ products).
General project management skills.
Good oral and written communications skills.
Good collaborative skills and ability to work with a cross-functional team.
WHAT TAKEDA CAN OFFER YOU:
401(k) with company match and Annual Retirement Contribution Plan
Tuition reimbursement
Company match of charitable contributions
Health & Wellness programs including onsite flu shots and health screenings
Generous time off for vacation and the option to purchase additional vacation days
Community Outreach Programs
Empowering Our People to Shine
Learn more at 
takedajobs.com
Takeda is an EEO employer of minorities, women, disabled, protected veterans, and considers qualified applicants with criminal histories in accordance with applicable laws. For more information, visit 
****No Phone Calls or Recruiters Please.
LI-KL1
Locations
Boston, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time >
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