
51 - 200 employees
💰 $135M Series C on 2021-02
Vividion Therapeutics, Inc. is a biotechnology company focused on transforming the future of human health through the creation of highly selective small molecule medicines that drug traditionally inaccessible targets. The company is advancing a broad, diversified pipeline of multiple, selective small molecule therapeutics for highly sought-after disease-causing target proteins in oncology and immunology. The company’s cutting-edge platform was spun out of the labs of Vividion’s scientific founders, a team of experts in chemical biology and synthetic chemistry from The Scripps Research Institute in La Jolla, CA.
🔥 38 minutes ago
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51 - 200 employees
💰 $135M Series C on 2021-02
Vividion Therapeutics, Inc. is a biotechnology company focused on transforming the future of human health through the creation of highly selective small molecule medicines that drug traditionally inaccessible targets. The company is advancing a broad, diversified pipeline of multiple, selective small molecule therapeutics for highly sought-after disease-causing target proteins in oncology and immunology. The company’s cutting-edge platform was spun out of the labs of Vividion’s scientific founders, a team of experts in chemical biology and synthetic chemistry from The Scripps Research Institute in La Jolla, CA.
• Provide support to clinical trials or other scientific research studies. • Assist with development of statistical analysis plans, Mock TFL shells (or product safety analysis plans/integrated summary of safety analysis plans/analysis plans for GMA evidence generation) with details for programming implementation. • Under supervision, help to oversee and QC CRO’s work. • Collaborate with Statistical Programming and work on QCing of internal programming outputs to ensure the delivery of high-quality outputs according to agreed-upon timelines. • Assist in identifying scientifically appropriate data collection instruments. • Identify and report data issues or violations of study assumptions. • Provide programming specifications for derived variables and analysis datasets. • Collaborate with Data Management in preparing for database lock. • With supervision perform statistical analyses as per the analysis plan. • Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures. • Ensure the accuracy of the statistical component of scientific reports and/or publications with high quality. • Work collaboratively with cross-functional teams, such as DM, medical team, PK/PD teams.
• MS (with 10+ years of experience) or PhD (with 7+ years of experience) in Statistics, Biostatistics, or a highly related field. • High degree of technical competence and effective communication skills, both oral and written. • Strong SAS and/or R programming skill is a must. • Able to perform statistical computations and simulations. • Able to identify data or analytical issues and assist with providing solutions by either applying own skills and knowledge or seeking help from others. • Able to build strong relationship with peers and cross-functional partners to achieve higher performance. • Highly motivated to drive innovation by raising the bar and challenging the status quo.
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