
Legal • B2B • SaaS
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.
September 18
🇺🇸 United States – Remote
💵 $150k - $165k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor

Legal • B2B • SaaS
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.
• 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 to facilitate understanding of statistical services and product • 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 all deliverables and author appropriate sections of protocols, statistical analysis plans, CSRs, presentations, and publications • Lead, manage, and support statistical activities for clinical studies, submissions, and development initiatives • Track and escalate concerns related to changes in scope of services • Mentor junior biostatisticians
• Required: Bachelor's degree or international equivalent in Biostatistics, Statistics, or related field • Preferred: Master's degree or equivalent in Biostatistics, Statistics, or related field • 5 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 • Physical requirements: ordinary ambulatory skills; ability to stand, walk, stoop, kneel, crouch periodically; lift/carry 10-35 pounds; arm, hand and finger dexterity including typing for prolonged periods; visual acuity; ability to sit, reach, talk, and hear for prolonged periods • Equivalent experience, skills, and/or education will be considered
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