Job Description

JOB DESCRIPTION
Responsibilities:

Implements a wide variety of statistical methodologies

Presents statistical reports to DMCs and clients.

Provides guidance and oversight of biostatistics and programming teams in production of statistical analyses and reports, including interim analyses and adaptations, for DMCs.

Ensures blinding and security of data is maintained, as required by contract, charter, or protocol and in compliance with related SOPs and regulatory requirements.

Serves as primary contact for clients and DMCs.

Hosts DMC meetings and presents unblinded reports to the DMC in closed meeting sessions.

Leads and facilitates project team meetings on a regular basis.

Develops and facilitates internal and external presentations, as appropriate.

Interact and coordinate with non-DMC Cytel functional groups.

Qualifications:

Master’s degree or PhD in Biostatistics, Statistics, or related field.

With a PhD: 3+ years’ experience working with clinical trial data, preferably in a CRO environment. With a MS, 5+ years’ experience working with clinical trial data, preferably in a CRO environment.

Expert level knowledge of statistical concepts with working knowledge of medical/scientific terminology

Strong organizational and multi-tasking skills are required, as are excellent verbal and written communication skills.

Must read, write and speak English.

Prior DMC experience required.

Job Tags

Permanent employment, Contract work, Interim role,

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Senior DMC Biostatistician Job at Cytel - USA & APAC, Cambridge, MA

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