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Biostatistician

Job not on LinkedIn

🕒 October 1

🇺🇸 United States – Remote

💵 $115k - $130k / year

⏰ Full Time

🟢 Junior

🧪 Clinical Research

Where this job comes from

Posted on Lexitas Pharma Services's careers page, not through a job board

First seen by Remote Rocketship October 1

Still open on Lexitas Pharma Services's site. Checked 8 hours ago.

Logo of Lexitas Pharma Services

Lexitas Pharma Services

51 - 200 employees

Founded 2011

🏥 Healthcare

💊 Pharmaceuticals

🤝 B2B

Healthcare • Pharmaceuticals • B2B

Lexitas Pharma Services is a specialized full‑service clinical research organization (CRO) focused exclusively on ophthalmology. With over 15 years dedicated to eye disease and therapy development and a team (ophthalmologists, optometrists, clinical operations specialists, and imaging experts) claiming more than 475 years of combined ophthalmology and clinical research experience, Lexitas provides end‑to‑end clinical development services — including monitoring, data management, regulatory and medical writing, and an integrated Reading Center — tailored to sponsors across cornea-to-retina indications. They emphasize personalized services, rigorous quality standards, and operational support for clinical trials in ophthalmic subspecialties.

📋 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

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