Biostatistician Clinical Trials

As a full-time salaried employee, you will be responsible for:
- producing & quality control of statistical analysis plans,
- producing & quality control of derived (analysis) datasets,
- Producing & quality control of tables, listings & figures (TFLs) output in SAS,
- providing statistical advice to clients,
- Statistical input into protocols including trial design, sample size calculations
- statistical input into protocol & clinical study reports,
- Fulfilling the role of lead biostatistician on a clinical study as part of the project team.
- Interacting with clients as key contact with regards to statistical issues.
- Producing & quality control of descriptive & non-descriptive analysis
- Applying advanced statistical methods
- the Production & quality control of r&omizations
- the Production & quality control of statistical reports.
- Providing Input into CRF development .
- Writing statistical methodology sections for inclusion into study protocols.
- Using efficient SAS programming techniques.
- Reviewing publications & clinical study reports.
- Representing PAREXEL at client marketing & technical meetings.
- Mentoring & training junior members of the department

GROWTH:
While most companies were busy downsizing, PAREXEL added over 2100 employees in 2009 alone.

PROMOTION:
In 2009, more than 1200 PAREXEL employees received career promotions.

EXPERTISE:
PAREXEL's experts, who have experience across a broad range of therapeutic areas, have supported nearly all of the top 50 best selling drugs that are on the market today.

AWARDS:
Scrip Award for Best CRO, 2008
-BioSingapore Award for Best Performing CRO, 2009
-Good Clinical Practice Journal, Most Innovative Patient Recruitment Strategy, 2008
-Globe 100 - Top 10 Best-Performing Massachusetts-Based Public Company, 2009

Keywords: statistician, biostatistics, statistical, statistics, biostatistician, tables, listings, figures, sap, Bayesian, clinical trial, clinical study, clinical studies, biostatistics, clinical programming, bid defenses, client meetings, global trials, global studies, FDA, regulatory, medical writing, data management, contracts, proposals, pm, project management, project manager, implementation, client interaction, sponsor, pharma, biotech, rfp, rfi