Principal Statistical Programmer/Analyst Consultant Remote

ClinChoice

$125K — $150K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Minimum 10 years of SAS programming experience in the pharmaceutical/biotech field
  • BA/BS in computer science, statistics, or math; MA/MS with 8 years of experience acceptable
  • Strong expertise in SAS programming language and report generation
  • Experience with CDISC data standards is mandatory
  • Previous role as a senior statistical programmer in FDA-regulated environments
  • Familiarity with Clinical Study Reports and NDA submissions
  • Proficient communication skills for cross-functional team collaboration

Responsibilities

  • Participate in CRF design and database review
  • Produce data listings, summary tables, and graphics for analyses
  • Integrate data across studies and validate programs according to guidelines
  • Coordinate programming standards with CROs and vendors
  • Validate analysis datasets and TFLs from vendors
  • Collaborate with Biometrics functions on clinical trial data analysis
  • Handle ad-hoc requests and support manuscript and presentation development

Benefits

  • Supportive and quality-focused company culture
  • Opportunities for professional development
  • Client-facing role that enhances interpersonal skills
  • Experience in a diverse range of therapeutic areas
  • Flexibility of a remote work environment
Full Job Description
ClinChoice is searching for a Principal Statistical Programmer Consultant to join one of our clients.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client's counterparts.

Main Job Tasks and Responsibilities:

Participate in CRF design, database review, data management plan, data review, data validation procedures, and review of data listings;

Produce data listings, summary tables, and graphics for interim and final analyses;

Integrate data across studies within a project. Test, document, review, and validate all programs according to department guidelines;

Coordinate data transfer and/or programming standards with CROs and vendors. Validate analysis datasets and TFLs from vendors;

Collaborate with other Biometrics functions for all activities related to the analysis of clinical trial data;

Responsible for the execution of ad-hoc requests, manuscripts, posters, and presentations.

Requirements:

Minimum of 10 years of SAS programming in the pharmaceutical or biotechnology industry with a BA/BS in computer science, statistics, math, or MA/MS with 8 years of experience;

Expertise in SAS programming language, report generation, and standards for programming and validation;

Therapeutic area- Rare Disease

Experience with CDISC data standards required.

Experience as a senior statistical programmer at a pharmaceutical or CRO working in an FDA-regulated environment;

Experience with Clinical Study Reports and NDA submission;

Ability to work on multiple tasks simultaneously and meet project deadlines;

Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we have received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

#LI-#TT1 #LI-Remote #Principal #Contract

Similar Jobs

More Jobs at ClinChoice

More Pharmaceuticals & Biotech Jobs

Find similar Principal Statistical Programmer/Analyst Consultant Remote jobs: