Affiliated Board Member – Non-Scientific

Job not on LinkedIn

🔥 2 minutes ago

🇺🇸 United States – Remote

💵 $58.5k - $96.5k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🪙 Affiliate Manager

👻 Ghost score 0%

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Advarra

WebsiteLinkedInAll Job Openings

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.

📋 Description

• 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 core review activities while maintaining professionalism and regulatory compliance • Answer questions and solve day-to-day challenges with Advarra staff and other board members • 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 requiring guidance, inconsistencies in Board reviews, and similar issues to senior regulatory staff • Consult with sponsors, investigators, and CROs on clinical and regulatory affairs as necessary • Work with Regulatory Leadership to identify membership needs and develop Board members • Promote accountability through motivation, team building, training, mentoring, collaboration, and respect

🎯 Requirements

• 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 research regulations and guidance • Master’s Degree preferred • Certified IRB Professional (CIP) certification preferred • Ability to learn and comprehend basic instructions • Ability to focus and attend to tasks and responsibilities • Verbal communication, listening and understanding, responding, and speaking • 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. • Candidates must work remotely in the United States

🏖️ Benefits

• Variable bonus eligibility in addition to base salary • Health coverage • Paid holidays • Inclusive and collaborative workplace culture • Equal opportunity workplace