Top 3 Principal statistical programmer Jobs in Queens Ny

Senior Principal Statistical Programmer
Katalyst Healthcares & Life Sciences —Newark, NJ
- Contract
- 6 years
- Doctor of Philosophy
- Organizational skills
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Principal Statistical Programmer (Remote)
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Must have sound technical judgment and experience in process design and implementation in relevant areas. Perform hands on primary statistical programming and…
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Principal Biostatistician (Remote)
Everest Clinical Research —Bridgewater, NJ
Provide statistical oversight on projects in the assigned drug development programs/projects, ensuring sound statistical methodologies in study design, sample…
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Senior Principal Statistical Programmer

Katalyst Healthcares & Life Sciences -
Newark, NJ

Quick Apply

Job Details

Contract

Qualifications

SAS
Team leadership
Drug regulation
SAS language
Schedule management
ICH guidelines
CDISC standards
Managing clinical research teams
Clinical quality assurance standards
Achieving project delivery timelines
Leading research teams
Senior leadership

Full Job Description

Job Description:
The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing.
Responsibilities:

Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc.
Review CRF, database design, and edit check specs.
Review study quality surveillance plan and monitor study conduct.
Prepare and/or review SAP, TFL shells and specifications for variable derivation.
Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables.
Provide statistical and validation support for statistical analysis, analysis datasets and TFL.
Review study report, manuscripts and other documents related to statistics.
Work on responses to health authorities and execute new analysis required for responses, review statistical inputs for regulatory documents.
Perform other ad-hoc statistical activities as needed.
Works effectively with cross functional groups, study team, and vendors. Proactively control and monitor timelines related to statistics and statistical programming.
Participates in monitoring CRO activities and reviewing CRO deliverables Other duties as assigned.

Requirements:

Ph.D. or MS in Statistics or Biostatistics.
Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience.
Excellent knowledge of SAS computer package.
Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines.
Excellent organizational skills, time management, and ability to meet established deadlines.
Excellent communication and interpersonal skills to effectively interface with others.
Ability to work independently and problem-solve.
Ability to provide leadership for the CRO statisticians and statistical programmers.

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