Clinical Statistician

3 weeks ago

Chennai, India Pfizer Full time

ROLE SUMMARY

Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide statistical expertise on regulatory submissions and ensure quality and appropriateness of submission deliverables under the supervision of senior statistical staff. Provide statistical expertise in maximizing the value of aggregate clinical data in support of scientific and drug development strategies under the supervision of senior statistical staff. Provide study level statistical expertise and communicate resource needs to management and other line functions for the execution of statistical tasks.

ROLE RESPONSIBILITIES

Through effective partnership with lead project statistician, provide statistical input to study designs, statistical analysis plans, interpretation of statistical results, project development plans, regulatory issues and scientific and commercialization projects Provide planning, delivery and communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results , support for publication activities , scientific presentations, and support to product defense. Accountable for study level and submission level statistical deliverables on assigned projects. Develop effective collaborations and sound working relationships with others within GPD Ensure that all study and project level statistical activities are conducted in compliance with relevant regulatory requirements and Pfizer standards. Provide statistical input to cross-functional activities – collaborate with other statisticians, study managers, and other colleagues for assigned studies and regulatory submissions Provide input to management plans to support assigned studies and submissions. Ensure timeliness and quality of statistical deliverables according to project plans for assigned studies and projects. Ensure tracking of clinical trial/allocated project activities and milestones. Participate in non-clinical project activities as needed Comply with all statistics and quality processes and standards that are applicable to statistical outputs, and support processes that require statistical input. Communicate and collaborate with other project statisticians within the therapeutic area to ensure consistency of statistical approaches Participate in research on statistical methodology and its applications pertinent to business needs.

BASIC QUALIFICATIONS

Advanced degree (Masters, PhD) in Statistics, Biostatistics, or related field. 3-6 yrs relevant experience in clinical trials is desirable but not necessary. Strong statistical skills with application to clinical trials. Effective verbal and written English communication skills in relating to colleagues and associates both inside and outside the organization.

PREFERRED QUALIFICATIONS

Working knowledge of SAS, R

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical#LI-PFE

  • Clinical Statistician

    1 month ago

    Chennai, India Pfizer Full time

    ROLE SUMMARY - Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. - Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. - Provide...

  • Clinical Statistician

    2 weeks ago

    chennai, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide...

  • Clinical Statistician

    3 days ago

    Chennai, Tamil Nadu, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide...

  • Clinical Statistician

    3 days ago

    Chennai, Tamil Nadu, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide statistical...

  • Clinical Statistician

    3 weeks ago

    Chennai, Tamil Nadu, India Pfizer Full time

    ROLE SUMMARY - Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. - Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. - Provide...

  • Clinical Statistician

    2 weeks ago

    Chennai, India Pfizer Full time

    Role Summary: - Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, standards and best practices. - Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. - Provide statistical...

  • Clinical Statistician

    2 months ago

    Chennai, India Pfizer Full time

    Role Summary: - Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. - Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. - Provide...

  • Clinical Statistician

    3 days ago

    Chennai, Tamil Nadu, India Pfizer Full time

    Role Summary: Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide statistical...

  • Clinical Statistician

    3 days ago

    Chennai, Tamil Nadu, India Pfizer Full time

    Role Summary: Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide statistical...

  • SAS Consultant with Pharmaceutical ...

    2 months ago

    chennai, India Anicalls (Pty) Ltd Full time

    • Excellent understanding of the statistical principles underlying clinical trials• Excellent statistical skills.• candidates that are Statistical SAS, R programmers, and separately, we need pharmaceutical clinical trial statisticians.• Excellent understanding of the regulatory issues associated with the reporting of clinical data in the submission...

  • Principal Biostatistician

    4 weeks ago

    Chennai, India Pfizer Full time

    ROLE SUMMARYDesign, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices.Provide statistical expertise and contributions for projects and protocols in support of clinical development.ROLE RESPONSIBILITIESProvide statistical input to study designs,...

  • Principal Biostatistician

    3 days ago

    Chennai, Tamil Nadu, India Pfizer Full time

    ROLE SUMMARYDesign, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices.Provide statistical expertise and contributions for projects and protocols in support of clinical development.ROLE RESPONSIBILITIESProvide statistical input to study designs,...

  • Principal Biostatistician

    3 days ago

    Chennai, Tamil Nadu, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development. ROLE RESPONSIBILITIES Provide statistical input to study...

  • Principal Biostatistician

    4 weeks ago

    Chennai, Tamil Nadu, India Pfizer Full time

    ROLE SUMMARY- Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices.- Provide statistical expertise and contributions for projects and protocols in support of clinical development. ROLE RESPONSIBILITIES- Provide statistical input to study designs,...

  • Principal Biostatistician

    19 hours ago

    Chennai, Tamil Nadu, India Pfizer Full time

    ROLE SUMMARY- Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices.- Provide statistical expertise and contributions for projects and protocols in support of clinical development. ROLE RESPONSIBILITIES- Provide statistical input to study designs,...

  • Principal Biostatistician

    4 weeks ago

    Chennai, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development. ROLE RESPONSIBILITIES Provide statistical input to...

  • Principal Biostatistician

    2 weeks ago

    Chennai, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development. ROLE RESPONSIBILITIES Provide statistical input to...

  • Principal Biostatistician

    4 weeks ago

    chennai, India Pfizer Full time

    ROLE SUMMARY Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development. ROLE RESPONSIBILITIES Provide statistical...

  • Senior Biostatistician

    2 months ago

    chennai, India Anicalls (Pty) Ltd Full time

    • Coordinate and lead a project team to the successful completion of a project within timelines and budget• Interact with clients as crucial contact about statistical and Full Time/Permanentual issues• Perform QC of derived datasets, tables, figures, and data listings produced by other department members and your own to ensure first-time quality•...

  • Principal Statistical Data Scientist

    2 weeks ago

    chennai, India Pfizer Full time

    Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field. At least 5 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency. Statistical Programming and SAS hand-on experience Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial...