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Biostatisticians

Eingestellt von Bio Careers

Gesuchte Skills: Support, Design

Projektbeschreibung

FORTUNE 100 PHARMA CLIENT HAS SEVERAL OPENINGS FOR BIOSTATISTICIANS (BIOSTATISTICIAN, SR. BIOSTATISTICIAN, MGR BIOSTATISTICS, SR. MGR BIOSTATISTICS). EXCELLENT BENEFITS!!

Successful candidates implement and execute methodological and statistical aspects of clinical studies with direction from Therapeutic Area lead or project lead statistician. Provide leadership and guidance on statistical matters to interdepartmental clinical / regulatory teams. In some cases principal function could be to develop / employ technical expertise in a particular statistical area or application.THERAPEUTIC AREA: ONCOLOGY. PHASE EXPERIENCE: PHASE I

KEY RESPONSIBILITIES:

- SUPPORT/PARTICIPATE IN THE DEVELOPMENT OF CLINICAL PROGRAM.
- REVIEW PROTOCOLS AND CRFS FOR SOUNDNESS OF TRIAL DESIGN.
- WRITE STATISTICAL METHODOLOGY SECTION OF THE PROTOCOL.
- PREPARE ANALYSIS PLAN AND PROGRAMMING SPECIFICATIONS
- Perform inferential analyses; inputs to the statistical section of the clinical study report and review clinical study report
- Support/participate in project related activities including preparation of BLA submissions and oversee CRO deliverables for studies contracted out.

RESPONSIBILITIES:

- With periodic supervision and guidance from senior departmental staff, provide support and leadership to a clinical study team on all relevant statistical matters.
- Act as liaison to study team, ensuring that the clinical study is conducted in a manner that supports planned statistical analysis.
- With some supervision and guidance from senior departmental staff, design clinical study and help produce protocol or
- amendments. Perform relevant sample size calculations.
- Develop statistical analysis plan (SAP).
- Work with programming team to provide definitions, documentation, and review of derived variables needed to produce planned TFL.
- Perform statistical analysis defined in SAP, prepare statistical methods and results sections for the clinical study report (CSR), and work with the study team to move the CSR through review and approval process.
- Provide statistical insight into interpretation and discussion of study results.
- Produce / coordinate production of statistical summaries ,analyses, annual reports, and related materials for submission to
- regulatory authorities or independent monitoring committees.
- Provide assistance to project Biostatistician or Therapeutic Area lead Biostatistician in project activity and timeline tracking, resource planning, and preparation of scientific reports or position papers.

Projektdetails

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Bio Careers