
1001 - 5000 employees
☁️ SaaS
📋 Compliance
🤝 B2B
💰 $100M Post-IPO Equity - Revance Therapeutics on 2024-03
SaaS • Compliance • B2B
Revance is the company name provided, but the supplied information appears to describe accessiBe. accessiBe is an expert-driven, AI-powered web accessibility company that provides automated remediation (accessWidget), accessibility scanning and developer tools (accessScan, accessFlow), manual expert audits and user testing, file/PDF accessibility, litigation support and attorney consultation, training and white-label partner programs, and integrations with major CMS and e-commerce platforms. The company emphasizes WCAG/ADA/EAA compliance, continuous automated updates, SOC2-level security, and sells subscription plans for small businesses through enterprise customers.
🔥 55 minutes ago
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1001 - 5000 employees
☁️ SaaS
📋 Compliance
🤝 B2B
💰 $100M Post-IPO Equity - Revance Therapeutics on 2024-03
SaaS • Compliance • B2B
Revance is the company name provided, but the supplied information appears to describe accessiBe. accessiBe is an expert-driven, AI-powered web accessibility company that provides automated remediation (accessWidget), accessibility scanning and developer tools (accessScan, accessFlow), manual expert audits and user testing, file/PDF accessibility, litigation support and attorney consultation, training and white-label partner programs, and integrations with major CMS and e-commerce platforms. The company emphasizes WCAG/ADA/EAA compliance, continuous automated updates, SOC2-level security, and sells subscription plans for small businesses through enterprise customers.
• Reporting to the Medical Science Liaison - Therapeutics. • Develop and maintain professional relationships with external stakeholders to support their scientific and data needs. • Facilitate information exchange, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies. • Serve as subject matter expert and provide fair-balanced, objective, scientific information and appropriate product education. • Responsible for maintaining monthly expenses to assigned budget parameters. • Conduct all field scientific support activities under the direction of Medical Affairs leadership in accordance with current regulatory and healthcare compliance guidelines.
• PhD, MD, PharmD, DO or other recognized doctorate level education. • Minimum of 3 years MSL experience (5 years preferred); preferably with expertise in neuromodulators (botulinum toxin/neurotoxins/movement disorders) and/or other relevant specialties, and minimum of 5 years post professional degree, practice, or relevant transferrable experience (e.g., clinical practice, academic research, regulatory/scientific). • Experience, desire, and initiative to deliver superior services to internal and external stakeholders. • Knowledge of customer segments and market dynamics within Movement disorders. • Highly-developed interpersonal skills and demonstrated ability to develop and maintain credible medical / scientific relationships with TLs in Neurology and Physiatry. • Capability to work independently or in a cross-functional team structure and to adjust effectively to work within new structures, processes, requirements, or cultures. • Working knowledge of drug development, regulatory approval processes, clinical trial methodologies, and guidelines. • Knowledge of PhRMA, OIG, and other regulatory guidelines relating to compliant medical and scientific communications.
• $175,000-$190,000 annual base salary and annual performance bonus. • Flexible PTO, holidays, and parental leave. • Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!
Apply Now🔥 1 hour ago
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