Affiliated Board Member – Non-Scientific

Advarra

. Maintain superior knowledge of regulatory requirements, Advarra’s Board Standard Operating Procedures, and Organizational Policies and Procedures .

Posted 10/16/2026full-timeRemote • United StatesMid-LevelSenior💰 $58,495 - $96,517 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in regulatory compliance and Institutional Review Board (IRB) processes, with a strong focus on collaboration, mentorship, and effective communication within clinical research environments.

Highest-signal resume keywords

Regulatory ComplianceInstitutional Review Board (IRB) ExperienceCertified IRB Professional (CIP)Clinical Research KnowledgeVerbal Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory Requirements KnowledgeResearch Regulations UnderstandingSubmission ReviewProtocol PresentationProblem Solving

Soft Skills

Team BuildingMotivationMentoringCollaborationAttention to Detail

Certifications & Qualifications

Certified IRB Professional (CIP)

Industry Keywords

Clinical ResearchHealthcare ExperienceBoard Standard Operating ProceduresOrganizational PoliciesInstitutional Review Board

About the role

Key responsibilities & impact

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

What you’ll need

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

Comp & perks

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