Principal Statistical Programmer

August 28

Apply Now

Receive Emails with Similar Jobs

Catalyst Clinical Research

WebsiteLinkedInAll Job Openings

Listen, Devise, Breakthrough

Clinical Operations Services • Clinical Resourcing/Staffing • Clinical Teams • Functional Service Provider

201 - 500

Description

• Program routine and customized data displays using SAS • Creation of safety and efficacy SAS datasets • Creation of project specific macros and formats • Performing data checks to ensure integrity and correctness of data displays • Perform QC/validation of datasets, tables, listings, figures • Establish and maintain professional working relationships • Represent department in multi-disciplinary settings • Ensure the quality and integrity of data analysis and reporting • Maintain awareness of project budgets and tasks • Contribute to the development of functional-level standards, tools, and templates • Interact across operational areas as required

Requirements

• Bachelor's Degree in Computer Science/Mathematics or equivalent • MS preferred • Hands on Experience with CDISC/SDTM/ADaM Programming • A minimum of 5 years SAS programming experience • Previous experience in a pharmaceutical research or CRO setting • Proficient with Microsoft Office Suite • Excellent written and oral communication skills • Excellent presentation skills • Strong organizational, problem-solving, and analytical skills • Ability to manage priorities and workflow • Versatility, flexibility, and a willingness to work within constantly changing priorities • Proven ability to handle multiple projects and meet deadlines • Strong interpersonal skills • Ability to deal effectively with a diversity of individuals at all organizational levels • Commitment to excellence and high standards • Creative, flexible, and innovative team player • Ability to work independently and as a member of various teams and committees • Good judgement with the ability to make timely and sound decisions • Ability to be discrete with sensitive company information • Knowledge of clinical trial study design • Can attend study meetings as needed