
1001 - 5000 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $75M Private Equity Round on 2015-12
Biotechnology • Healthcare Insurance • Pharmaceuticals
Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.
🕒 February 26
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1001 - 5000 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $75M Private Equity Round on 2015-12
Biotechnology • Healthcare Insurance • Pharmaceuticals
Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.
• Lead the development and optimization of clinical data systems • Drive data standardization and build validation frameworks • Design high-performance databases and pipelines across global trials • Architect scalable validation frameworks to proactively address systemic data issues • Build and maintain modular codebases, set coding standards, and mentor junior engineers • Oversee regulatory alignment with GCP and FDA 21 CFR Part 11 • Develop dynamic dashboards and analytics tools to deliver actionable insights into trial performance and data quality • Act as a strategic liaison across Biostatistics, Clinical Operations, and Regulatory Affairs
• Bachelor’s Degree in a relevant field (life sciences, statistics, data management, clinical operations) or relevant/equivalent combination of education, training, and experience • Minimum 6 years experience in clinical monitoring, clinical trial management or equivalent • Advanced programming and automation skills; database design; dashboard development; CDISC governance • Professional working proficiency in English • Highly effective oral and written communication skills with the ability to communicate effectively with project team members • Excellent organizational and time management skills • Ability to work in a team or independently as required • Demonstrated ability to learn how to extract pertinent information from protocols, electronic study data systems and clinical systems • Proficiency in statistical analysis and data monitoring tools • Detail-oriented with strong analytical and problem-solving skills • Demonstrated experience with integrated risk planning & management • Ability to mentor junior team members • Preferred: CRO experience as a Clinical Data Engineer or Programmer
• Health insurance • Retirement plans • Paid time off • Flexible work arrangements • Professional development
Apply Now🕒 February 26
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