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Principal Statistical Programmer

5.00 to 7.00 Years   Chennai   27 Apr, 2023
PFIZER LIMITED
Job LocationChennai
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

    locations India - Chennai India - Mumbai time type Full time posted on Posted 30+ Days Ago job requisition id hidden_mobile JOB SUMMARY
    • Hands on programming role, supporting deliverables in the study/project/portfolio/standards team, of medium or high complex statistical programming deliverables
    • Mentored/Guided by Statistical Programming Leads within Standards/Study/Project/Portfolio/TA s
    • Guide, mentor, monitor programmers within the team and collaborate with SPL s on timelines, resource management and deliverables with quality.
    • Work collaboratively with study teams and stakeholders such as clinicians and statisticians on milestones and deliverables.
    JOB RESPONSIBILITIES
    • Accountable for multiple projects/ongoing work activities (timelines, work plans, deliverables) of moderate complexity within a Work Team
    • Accountable for their assigned work supporting the standards/study deliverables and also to assist SPL s with the team assignments.
    • Develop/Validate/Review datasets, TFL as per CDISC aligned to the company Standards or company Data Standards for Study/Project/Portfolio. (Portfolio)
    • Explore the existing code base and execute/perform runs as required, also develop/modify/review as per the needs and specifications suggested to the standards team as appropriate (Standards)
    • Regularly update leads on progress and time estimations to ensure smooth daily operations and accurate planning
    • Acts as mentor to junior team members
    QUALIFICATIONS & SKILLS
    • 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 data
    • Working knowledge of clinical data and relevant data standards
    • Strong written and oral communication skills, and project management skills
    • Knowledge of at least 1 Therapeutic Area
    • CDISC and submission experience desirable.
    Location: Chennai, MumbaiPfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Medical #LI-PFE,

Keyskills :
sassas programmingsdtmdata managementreportingequal employment opportunityclinical datadata standardsdaily operationsproject managementoral communicationresource managementcommunication skillslegislative relationsproject administrationstati

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