Principal Statistical Programmer/Analyst Consultant Remote

ClinChoice

6d•Remote

About The Position

ClinChoice is searching for a Principal Statistical Programmer Consultant to join one of our clients. This is a client-facing role where candidates are expected to work independently while establishing a high-trust environment with the client’s counterparts. The role involves working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring.

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.
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.

Nice To Haves

Therapeutic area: Rare Disease

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.