Compliance Analyst

Vaga não está no LinkedIn

🕒 Setembro 26

🦀 Maryland – Remoto

🦀 Maryland – Remote

💵 $85.344 - $98.145 / ano

⏰ Tempo Integral

🟡 Pleno

🟠 Sênior

🚔 Conformidade

👻 Score fantasma 0%

O que significa: quão provável esta vaga está aberta sem contratação ativa.Como ler: 60% ou mais significa que achamos que é uma vaga fantasma. Pontuações mais baixas preocupam menos.Como pontuamos: tempo em aberto, republicações, vagas abertas vs tamanho do time, rapidez para fechar vagas, e se o salário está divulgado.Observação: é uma estimativa de dados públicos, não um julgamento da empresa. Vagas reais podem ter pontuação alta, então use como uma dica, não como um fato.

Candidatar-se

Encontrar Vagas Remotas Similares

Configurar Alerta de Email para Novas Vagas

📊 Verifique sua pontuação de currículo para esta vaga

Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

Enviar Currículo

Ripple Effect

SiteLinkedInTodas as Vagas

51 - 200 funcionários

📣 Marketing

🏥 Saúde

📦 Logística

Marketing • Healthcare • Logistics

A Ripple Effect é uma empresa de consultoria especializada em fornecer serviços de consultoria de primeira linha e talentos nos setores federal, privado e sem fins lucrativos. Estabelecida em 2003, a Ripple Effect é reconhecida por seu papel em moldar políticas e programas que definem a nação. A empresa oferece uma ampla gama de serviços, incluindo gerenciamento de programas, suporte técnico e científico, comunicações e alcance, pesquisa e avaliação e transformação digital. Com foco em entregar resultados impactantes, a Ripple Effect possui uma equipe multidisciplinar de especialistas pronta para aprimorar as operações de negócios e promover o sucesso de seus clientes. Além disso, a empresa enfatiza a diversidade e a inclusão e foi reconhecida como uma das melhores e mais brilhantes empresas para se trabalhar no país. Seu trabalho abrange vários setores, demonstrando seu compromisso com a excelência e flexibilidade em atender às necessidades dos clientes.

Descrição

• Serve as first point of contact for communications between internal and external parties • Receive and review complaints and incident reports for completeness, accuracy, participant safety concerns, and regulatory significance • Provide preliminary assessments of complaints and incident reports to agency leadership • Draft correspondence, information requests, case summaries, briefing materials, status reports, communication logs, trackers, briefing decks, and training materials • Communicate with research institutions, IRB personnel, investigators, complainants, and government officials • Request and collect additional information for compliance evaluations • Present analyses and recommendations to supervisors and compliance review teams • Participate in internal case review meetings and support leadership reporting • Track case status, milestones, correspondence, and follow-up activities • Maintain records supporting transparency, quality assurance, and audit readiness • Ensure deliverables meet quality, format, content, and accessibility standards • Apply regulatory and contractual requirements to compliance procedures • Monitor and communicate institutional corrective actions and compliance resolutions • Analyze research documentation, IRB records, investigator information, and institutional responses • Contribute to process improvements and solutions for complex issues • Work independently under general direction and keep the supervisor updated • Perform other job-related duties as assigned

🎯 Requisitos

• Master's degree in public health, clinical research, health sciences, biomedical sciences, regulatory affairs, law, public administration, or a related field • 4+ years relevant experience; additional education substitutes for experience • Demonstrated experience related to human subjects research protections and regulatory compliance • Experience reviewing or supporting compliance activities related to human subjects research • Experience working with Institutional Review Boards (IRBs), Human Research Protection Programs (HRPPs), research compliance offices, or regulatory oversight organizations • Knowledge of federal regulations governing human subjects research, including 45 CFR 46 (Common Rule) • Experience evaluating research protocols, incident reports, complaints, audit findings, or compliance documentation • Experience preparing written analyses, regulatory summaries, reports, or compliance correspondence • Experience managing sensitive information and maintaining detailed records accurately • Basic knowledge of project management software such as Microsoft Planner, Microsoft Project, Asana, and Smartsheet • Exceptional attention to detail, ability to execute instructions, and commitment to quality and compliance • Intermediate experience with Microsoft Office productivity software and collaboration tools such as Microsoft Teams and SharePoint • Certificates in project management, CIP, CCRP, CHRC, or related research compliance credential recommended • Foundational technical writing knowledge for process documentation, briefing decks, status reports, memos, and business writing • Basic knowledge of AI tools, including limitations, risks, and project-management applications • Experience in academic medical centers, research institutions, federal agencies, or compliance oversight organizations • Familiarity with electronic compliance or case management systems and document management tools • Public Trust clearance

🏖️ Benefícios

• Diverse and engaging work environment • Meaningful opportunities to support an important public health mission • Flexible work options that support your lifestyle and professional growth • Competitive pay • Exceptional benefits • Programs supporting work/life balance and personalized preferences