Principal Programmer, Statistical Programming

Job not on LinkedIn

🔥 16 hours ago

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $149.2k - $223.8k / year

⏰ Full Time

🔴 Lead

🖥 Software Engineer

👻 Ghost score 20%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Lifelancer

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2020

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Pre Seed Round on 2022-03

Consulting • Healthcare • Logistics

Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.

📋 Description

• Work with management to delegate tasks appropriately and track progress • Provide expert technical support to team members • Serve as project lead Statistical Programmer on clinical sub-teams • Use advanced SAS features, including interfaces with software applications and operating system tools • Perform quality control checks of SAS code and output produced by other Statistical Programmers • Solve complex clinical trial reporting problems • Support daily operations and ensure study tasks are completed accurately and timely • Engage with Statistical Programmers, Biostatisticians, Data Management, and other departments, often at Senior Management levels • Create files, documents, and analyses required for electronic submissions in eCTD format, including ISS/ISE • Provide leadership for compliance with Vertex SOPs and FDA/ICH/GCP regulations • Create, review, and approve documentation supporting data analysis, reporting, and CDISC data submission • Participate in cross-functional project management teams working on SOPs, guidelines, process improvements, system validation and acquisition, and implementation and integration of tools and technologies

🎯 Requirements

• Bachelor’s degree in a scientific discipline • Typically 5+ years of work experience for M.S. or above, or 8+ years for B.S. • Work experience in biotech, pharmaceuticals, or a clinical research organization • Proficiency in SAS language, procedures, and functions commonly used in clinical trial reporting • Proficiency in SAS Macro language, BASE SAS, SAS/STAT, and SAS/GRAPH • Intermediate knowledge of CDISC standards • Intermediate knowledge of clinical trials • Regulatory submission experience • Effective written and verbal communication skills • Knowledge of clinical development and medical data • Experience with eCTD submissions, including ISS/ISE • Knowledge of Vertex SOPs and FDA/ICH/GCP regulations

🏖️ Benefits

• Annual bonus eligibility • Annual equity awards • Overtime pay eligibility in accordance with federal and state requirements • Medical benefits • Dental benefits • Vision benefits • Generous paid time off • Week-long company shutdown in the Summer and the Winter • Educational assistance programs including student loan repayment • Commuting subsidy • Matching charitable donations • 401(k) • Flexible work options through Remote-Eligible Flex Designation