Associate Director Biostatistics New Jersey

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Associate Director Biostatistics
This ‘hands-on’ leadership position which could be remote or based.
Core Responsibilities:

Ensure successful completion of programming (tables, listings, and graphs) for statistical deliverables

Provide estimates for proposals and contracts

Consult/review/write statistical sections of protocols

Assist in protocol study design (determine sample sizes for all phases of trials )

Write Statistical Analysis Plans (SAP)

Review/design CRFs

Review/write Randomization and Blinding Plans

Review/write charters for Data Monitoring Committee (DMC)

Provide SAS code for  statistical models

Validate/perform SAS programming for key data analyses

Perform quality control on derived variables  being analyzed

Interpret results from analysis

Maintain documentation

Review Clinical Study Reports (CSR)

Provides guidance and direction to team members to ensure departmental and client/project goals are met

Utilizes metrics to drive and enhance performance

Coaches develops and provides continuous feedback to team members

Additional duties as assigned by Global Head, Operations

Experience and Skill Requirements:
The successful candidate will hold a Master’s degree in Biostatistics and have 5+ years of relevant statistical experience in a pharmaceutical and/or CRO environment. Must have a firm knowledge of appropriate statistical methods and statistical analysis plans as well as a strong proficiency in SAS and sample size software.  Oncology experience is required.
The position requires an individual with highly developed leadership skills, strong analytical skills and proven ability to deliver results. Must possess a forward-thinking approach and be able to anticipate challenges and proactively implement solutions. The ability to handle multiple tasks simultaneously, prioritize and work under tight deadlines is required.  Excellent communication skills are essential for interaction with both internal and external clients.

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