Support B&SR/clinical trial team, take responsibility for deliverables on
programming activities and/or statistical aspects on clinical data of Phase I
–IV oncology trials under senior guidance.
Key Result Areas
1. Provide input as required at all meetings, discussions and activities
covering aspects of Statistical Reporting on trial level activities.
2. As required, make certain that documents and specifications are consistent
and comply with company standards by providing input into Case Record Form
(CRF), pooled datasets, data structures, specifications of analysis datasets,
listings, summaries, figures and tables for phase I – IV clinical trials
3. Program, according to specifications, analysis datasets, listings, tables,
and figures for phase I-IV clinical trials and also pooled datasets for Summary
of Clinical Safety and Efficacy.
4. Conduct reporting statistical tasks on assigned clinical trials e.g.Report
Analysis Preparation (RAP).
5. Track clinical trial milestones for Biostatistics & Statistical
Reporting (B&SR) deliverables.
6. Maintain records for all assigned studies including archiving of trial
analysis and associated documentation.
7. Support senior members of B&SR in maintaining efficient interfaces with
internal and external customers.
8. Comply with pre-defined project / study standards and specifications.
9. Support B&SR colleagues in non-clinical initiatives.
Minimum requirements:
0-4 years of relevant work experience with Masters degree in statistics or
computer science. Working knowledge and experience with SAS software.
Intermediate knowledge of office tools
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