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Company

Original Job Post

Cytel · 2 days ago

Senior Statistical Programmer

Upper Gwynedd, PA

Full-time

Hybrid

Senior Level

5+ years exp

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Hiring Manager

Claire Reid

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Responsibilities

Working under the direction of the Team Lead / Project Manager to conduct programming activities for trials and projects.

Leading study teams by providing technical and domain-related guidance.

Leading and managing a team of 2-4 members.

Working on SDTM and data migration from legacy datasets to standards like CDISC.

Preparing SAS analysis datasets, tables, listings, and figures as per specifications.

Creating programs for graphs and tables required in various reports.

Validating and transforming datasets as per client assignment specifications.

Coordinating with clients and teams for clarity on specifications and data issues.

Contributing to the recruitment process by identifying resource needs and conducting interviews.

Performing tasks using standard operating procedures and quality management systems.

Qualification

Find out how your skills align with this job's requirements. If anything seems off, you can easily click on the tags to select or unselect skills to reflect your actual expertise.

SDTMCDISCSASData MigrationProgram SpecificationsData ValidationQuality ManagementRegulatory RequirementsDrug DevelopmentClinical TrialsSOPs

Required

BS or MS degree in Computer Science, Statistics, or related health science field with a minimum of 5 years of SAS programming experience with clinical trial data

Proficiency of working on SDTM is mandatory

Ability to work on data migration from legacy datasets to standards such as CDISC or any other client-specific standard

Read and understand the program specifications document

Prepare SAS analysis datasets, tables, listings, and figures as per specifications

Create programs to create graphs and tables that are required in CSRs, safety reports, efficacy reports, etc. ensuring on-time quality delivery

Validate and transform datasets as per client assignment specifications

Validate tables, listings, and figures as per client assignment specifications

Coordinate with the client and US team for clarity of specifications, data issues, outliers, reviews, schedules, etc

Perform all tasks using standard operating procedures (SOPs) as defined in the Quality Management System or the respective client(s) as applicable

Well-conversed with regulatory requirements and drug development process

Good understanding of the Clinical trial domain and good SAS programming skills

Ability to work independently

Company

Cytel

Glassdoor

3.9

Cytel enables decision-makers in the life sciences to unlock the full potential of their products.

Founded in 1987

Cambridge, Massachusetts, USA

1,001-5,000 employees

http://www.cytel.com

H1B Sponsorship

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