Biostatistician

Job not on LinkedIn

🔥 2 minutes ago

🇺🇸 United States – Remote

💵 $115k - $130k / year

⏰ Full Time

🟢 Junior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Lexitas

WebsiteLinkedInAll Job Openings

501 - 1000 employees

🛡️ Insurance

💼 Consulting

📦 Logistics

💰 Debt Financing on 2016-09

Insurance • Consulting • Logistics

Lexitas is a trusted provider of legal and corporate support services, offering a wide range of services such as court reporting, record retrieval, legal talent outsourcing, registered agent services, process service, investigations, and eLaw case tracking. The company addresses the needs of legal, insurance, and corporate leaders by delivering responsive professional services combined with advanced technology solutions. Lexitas is dedicated to accuracy, timeliness, and reliability, making it an ideal partner for law firms, insurance companies, and corporations seeking to enhance efficiency and reduce costs in their legal and administrative operations.

📋 Description

• Inform the design, collection, analysis, reporting, interpretation, and publication of clinical trial data • Maintain a basic understanding of industry and academic developments in biostatistical methodology, regulatory trends, and ophthalmology • Support the development and rollout of new innovations, standards, processes, and efficiencies within Biostatistics • Provide scientific and technical consultation and collaborate with internal and external stakeholders • Support collaboration with Data Management • Review clinical trial data and validate key endpoints or datasets • Represent Lexitas in interfaces with Sponsors and vendors • Ensure consistency and adherence to standards and departmental SOPs • Ensure the statistical integrity of deliverables • Author appropriate sections of protocols, statistical analysis plans, CSRs, presentations, and publications of clinical trial data • Perform other tasks, duties, and job responsibilities as assigned

🎯 Requirements

• Bachelor’s degree or international equivalent in Biostatistics, Statistics, or related field • 1 or more years of experience in statistical analysis within clinical research, preferred • Basic understanding of statistical topics and methodology in drug and medical product development • Excellent technical and programming logic skills • Experience with cross-functional collaboration • Excellent verbal and written communication skills • Good planning and organizational skills with the ability to adapt and adjust to changing priorities • Ability to be productive and handle multiple tasks to meet deadlines in a dynamic, fast-paced environment • Strong interest in developing expertise in ophthalmology • Ability to perform the stated physical requirements, including lifting and carrying 10–35 pounds and prolonged standing, walking, sitting, reaching, typing, talking, and hearing • Equivalent experience, skills, and/or education will also be considered