
501 - 1000 employees
Founded 1983
🏥 Healthcare
💼 Consulting
☁️ SaaS
Healthcare • Consulting • SaaS
Advarra is a provider of integrated regulatory oversight and clinical trial technology, combining independent IRB review and compliance services with enterprise SaaS platforms (including Braid, OnCore, Clinical Conductor, eReg, and eSource). The company delivers operational intelligence, AI-powered protocol design and automation, site collaboration, study startup and enrollment tools, and strategic enablement services to sponsors, CROs, research sites, and institutions to improve efficiency, compliance, and patient safety across the clinical trial lifecycle.
🔥 15 hours ago
🇺🇸 United States – Remote
💵 $58.5k - $96.5k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🪙 Affiliate Manager
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501 - 1000 employees
Founded 1983
🏥 Healthcare
💼 Consulting
☁️ SaaS
Healthcare • Consulting • SaaS
Advarra is a provider of integrated regulatory oversight and clinical trial technology, combining independent IRB review and compliance services with enterprise SaaS platforms (including Braid, OnCore, Clinical Conductor, eReg, and eSource). The company delivers operational intelligence, AI-powered protocol design and automation, site collaboration, study startup and enrollment tools, and strategic enablement services to sponsors, CROs, research sites, and institutions to improve efficiency, compliance, and patient safety across the clinical trial lifecycle.
• Maintain superior knowledge of regulatory requirements, Advarra’s Board Standard Operating Procedures, and Organizational Policies and Procedures • Ensure Review Board compliance with regulatory requirements and organizational procedures • Help ensure timely execution of Institutional Review Board review activities while preserving professionalism and regulatory compliance • Answer questions and solve day-to-day challenges using scientific knowledge and regulatory expertise • Assist with triaging and reviewing submissions for expedited or full board review • Attend full board meetings and present protocol-related issues as needed • Identify areas for guidance, inconsistencies in Board reviews, and related issues to senior regulatory staff • Consult with sponsors, investigators, and CROs on clinical and regulatory affairs • Work with Regulatory Leadership to identify membership needs and develop Board members • Promote accountability through motivation, team building, training, mentoring, collaboration, and respect
• Bachelor's Degree • One (1)+ years of IRB or Clinical Research Industry experience preferred, OR minimum 3 years’ experience in healthcare within the last 6 years • Strong understanding of biological and/or pharmacological sciences through education or experience • Ability to sit or stand for extended periods at a stationary workstation • Ability to regularly carry, raise, and lower objects of up to 10 Lbs. • Ability to learn and comprehend basic instructions • Focus and attention to tasks and responsibilities • Verbal communication; listening and understanding, responding, and speaking
• Variable bonus eligibility • Health coverage • Paid holidays
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