Senior Statistical Programmer

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🔥 1 hour ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $104.8k - $128k / year

⏰ Full Time

🟠 Senior

🖥 Software Engineer

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WCG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💊 Pharmaceuticals

☁️ SaaS

💰 Private Equity Round - WCG on 2019-11

Healthcare • Pharmaceuticals • SaaS

WCG is a global clinical research services and technology company that supports sponsors, CROs, research sites, and institutions across the lifecycle of clinical trials. Founded as a leader in independent ethical review, WCG provides IRB and IBC review, data monitoring committees, site enablement and study start-up services, participant recruitment and retention, and data & insights (including benchmarking, statistical consulting, and AI-powered trial foresight). The company also offers a suite of technology platforms (e. g. , ClinSphere®, eReview Manager, Total Enrollment, Total Feasibility) and large protocol and performance datasets to help design, plan, and run trials more efficiently and compliantly. WCG positions itself as a partner to biopharma and medical research organizations to accelerate trial activation, improve enrollment, and ensure regulatory and ethical compliance.

📋 Description

• Develop, validate, and document SAS programs for clinical trial datasets (SDTM, ADaM) and outputs (tables, listings, figures) for regulatory submission, ensuring accuracy and compliance. • Lead programming activities and manage resources, timelines, and priorities for assigned studies and projects. • Conduct comprehensive quality control checks and peer code reviews on all programming deliverables. • Collaborate with statisticians, data managers, and clinical teams to ensure project requirements are met and deliverables are aligned. • Conduct thorough quality control checks on programs and datasets to ensure precision and dependability. • Oversee and manage programming activities for studies or projects, handling resource allocation, timelines, and budgets. • Guide junior programmers, offering mentorship on industry standards and best practices. • Provide expertise in interpreting and implementing Statistical Analysis Plan (SAP) programming specifications and project documentation. • Troubleshoot programming and data issues, resolve discrepancies, and ensure timely, reliable data reporting. • Coordinate multiple projects concurrently, setting strategic goals and adapting to evolving priorities. • Foster innovation within the department and contribute to process enhancement initiatives. • Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.

🎯 Requirements

• At least 5 years of SAS programming experience required. • R programming experience highly preferred. • 2 years of macro programming experience required. • At least 3 years of experience in the pharmaceutical, vaccines, biotech, or medical device industry required. • Phase 1- 4 clinical trials experience. • In depth knowledge of CDISC requirements required. • Understanding of Statistical Analysis Plan programming specifications. • Attention to detail, accuracy, initiative, and excellent communication skills are essential, as well as the ability to juggle several complex tasks simultaneously.

🏖️ Benefits

• Comprehensive Benefits package - Health, Dental, Vision, Life Disability, 401k with match, and flexible spending accounts • Employee Assistance Programs and additional work/life resources • Referral Bonuses and Tuition Reimbursement • Flexible PTO • Volunteer Time Off to benefit the community • Opportunities for career development with on-the-job training, certification assistance and continuing education reimbursement