Consultant, GxP Services

🕒 August 12

🇺🇸 United States – Remote

💵 $71k - $125k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

💼 Consultant

👻 Ghost score 10%

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Logo of Advarra

Advarra

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

• Support consultants in delivering GxP consulting services for pharmaceutical, biotechnology, medical device, and life sciences clients • Assist with planning and conducting domestic audits and assessments under senior team direction • Plan and perform independent audits with SME support • Support inspection readiness activities as a co-auditor • Participate in mock inspections with senior consultants • Assist with SOP reviews and documentation • Develop subject matter knowledge over time • Support client communications with the project team • Participate in continuous improvement initiatives • Perform consulting engagements under direction • Participate in investigator site, TMF, vendor, facility, document, and systems audits • Prepare audit documentation, reports, observations, and supporting project deliverables • Assist with quality control reviews of project documentation and data • Support inspection readiness activities, mock inspections, and compliance assessments • Participate in SOP reviews, gap analyses, and quality system improvement initiatives • Assist with developing client training materials and participate in delivery of GxP-related training as appropriate • Collaborate with project managers and senior consultants to meet project timelines and client expectations • Maintain current knowledge of applicable GxP regulations and industry best practices • Support internal process improvement initiatives and perform other duties as assigned

🎯 Requirements

• Bachelor’s degree in Nursing, Life Sciences, or related field (or equivalent combination of education and experience) • Minimum 3-5 years of experience in clinical research, quality assurance, regulatory compliance, or a related life sciences environment • Ability to travel extensively • 1-3 years of experience supporting GxP, QA, compliance, auditing, or operational functions • Experience working within pharmaceutical, biotechnology, medical device, CRO, or related industries • Foundational knowledge of GCP and other applicable GxP regulations focused on investigator sites • Spanish language skills – intermediate fluency • Demonstrated analytical and problem-solving skills • Strong written and verbal communication skills • Ability to manage multiple priorities while working collaboratively within project teams • Proficiency with Microsoft Office applications • 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 • Health coverage • Paid holidays • Equal opportunity workplace • Reasonable accommodation for applicants with disabilities

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