ToxStrategies, a BlueRidge Life Sciences Company
51 - 200 employees
Founded 2008
🔬 Science
💊 Pharmaceuticals
🤝 B2B
💰 Venture Round - ToxStrategies on 2023-01
Science • Pharmaceuticals • B2B
ToxStrategies is a multidisciplinary scientific consulting firm and BlueRidge Life Sciences company that provides toxicology, environmental, and regulatory science services to industry, government, and legal clients. The firm offers expertise in risk assessment, exposure assessment, computational toxicology, bioavailability, PFAS, micro- and nanoplastics, food and pharmaceutical safety, medical devices, NAMs, epidemiology, and regulatory compliance (e. g. , TSCA, FSMA, Proposition 65). ToxStrategies supports product stewardship, litigation support, and evidence-based toxicology across consumer products, chemicals, and biopharmaceutical contexts.
Vice President – Clinical Strategy
Job not on LinkedIn
🕒 March 14
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ToxStrategies, a BlueRidge Life Sciences Company
51 - 200 employees
Founded 2008
🔬 Science
💊 Pharmaceuticals
🤝 B2B
💰 Venture Round - ToxStrategies on 2023-01
Science • Pharmaceuticals • B2B
ToxStrategies is a multidisciplinary scientific consulting firm and BlueRidge Life Sciences company that provides toxicology, environmental, and regulatory science services to industry, government, and legal clients. The firm offers expertise in risk assessment, exposure assessment, computational toxicology, bioavailability, PFAS, micro- and nanoplastics, food and pharmaceutical safety, medical devices, NAMs, epidemiology, and regulatory compliance (e. g. , TSCA, FSMA, Proposition 65). ToxStrategies supports product stewardship, litigation support, and evidence-based toxicology across consumer products, chemicals, and biopharmaceutical contexts.
📋 Description
• Lead clinical operations programs providing vision, management, and execution • Achieve program goals via collaboration with all functional lines involved in clinical development • Provide operational leadership and execution of clinical trials according to regulatory guidelines • Oversee timelines, budgets, resources, clinical trial sites, and project deliverables • Continuous improvement of department infrastructure through SOPs and guidelines • Facilitate effective internal and external relationships to achieve project goals.
🎯 Requirements
• 10 years of progressive clinical operations/development experience in pharmaceutical/drug development • Preference for neurology/orphan drug experience • Proven track record of planning, conducting & managing clinical operations for Phase 1-4 studies • Experience managing clinical operations for drug across multiple therapeutic areas • Track record of leading a cross-functional team in a matrix environment • Demonstrated ability to handle a high volume of highly complex tasks within a given timeline.
🏖️ Benefits
• Comprehensive solutions addressing complex technical, clinical development, and regulatory challenges. • Integrated life sciences services spanning toxicology, regulatory science, epidemiology and clinical research.
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