Affiliated Board Member – Scientific

Advarra

. Maintain knowledge of and ensure Review Board compliance with regulatory requirements, Advarra’s Board Standard Operating Procedures, and Organizational Policies and Procedures .

Posted 10/19/2026full-timeRemote • United StatesMid-LevelSenior💰 $58,495 - $96,517 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in regulatory compliance and clinical research, with a strong understanding of biological and pharmacological sciences. Capable of effective communication and collaboration with diverse stakeholders in the clinical research environment.

Highest-signal resume keywords

Regulatory ComplianceClinical Research ExperienceBiological Sciences KnowledgeVerbal Communication SkillsTeam Building

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Regulatory RequirementsStandard Operating ProceduresClinical ResearchProtocol ReviewSubmission Review

Soft Skills

Problem SolvingMotivationCollaborationMentoringAttention to Detail

Industry Keywords

Institutional Review BoardHealthcare ExperienceScientific BackgroundCRO ConsultationAccountability

About the role

Key responsibilities & impact

Maintain knowledge of and ensure Review Board compliance with regulatory requirements, Advarra’s Board Standard Operating Procedures, and Organizational Policies and 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 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 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
Encourage 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 or other graduate level degree with an emphasis in a scientific background preferred
Strong understanding of biological and/or pharmacological sciences through education or experience
Superior knowledge of regulatory requirements, Advarra’s Board Standard Operating Procedures, and Organizational Policies and Procedures
Ability to learn and comprehend basic instructions
Focus and attention to tasks and responsibilities
Verbal communication; listening and understanding, responding, and speaking
Ability to regularly carry, raise, and lower objects of up to 10 Lbs.
Ability to sit or stand for extended periods of time at a stationary workstation

Benefits

Comp & perks

Variable bonus may be available in addition to base salary
Health coverage
Paid holidays
Equal opportunity workplace
Inclusive and collaborative work environment