Affiliated Board Member – Non-Scientific

Job not on LinkedIn

🔥 3 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

💼 Consulting

📦 Logistics

📣 Marketing

Consulting • Logistics • Marketing

Advarra is a provider of integrated technology and services for clinical research, combining institutional review and compliance services with software platforms to support the full clinical trial lifecycle. The company offers ethics review services (IRB, IBC, DMC, endpoint adjudication), site enablement and research staffing, and a suite of cloud products — including eRegulatory, eConsent, eSource/EDC, CTMS and study design tools — plus an AI-powered operational intelligence engine (Braid) to streamline trial start-up, enrollment, and operations. Advarra serves sponsors, CROs, research sites, and institutions with a focus on patient protection, regulatory compliance, and accelerating trial outcomes.

📋 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 preserving 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 • 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 • Master’s Degree preferred • Certified IRB Professional (CIP) certification preferred • Understanding of research regulations and guidance • 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

🏖️ Benefits

• Variable bonus eligibility in addition to base salary • Health coverage • Paid holidays