Director, Field Clinical and Patient Screening Programs

🕒 Outubro 21

🇺🇸 Estados Unidos – Remoto (EUA)

💵 $149.300 - $298.700 / ano

⏰ Tempo Integral

🔴 Especialista

👔 Diretor

🦅 Patrocina Visto H1B

Esta empresa já patrocinou vistos H1B no passado.

👻 Score fantasma 0%

O que significa: a chance de ninguém estar realmente contratando para esta vaga.Como ler: 60% ou mais significa que achamos que é uma vaga fantasma. Pontuações mais baixas preocupam menos.Por que essa pontuação:

• Aberta há 23 dias.
• As vagas desta empresa costumam ser preenchidas em 24 dias.

Candidatar-se

Adaptar currículo + carta de apresentação

Encontrar Vagas Remotas Similares

☆ Salvar☑️ Marcar como candidatado❌ Ocultar

Reportar problema

Abbott

SiteLinkedInTodas as Vagas

10.000+ funcionários

Fundada em 1888

🏥 Saúde

⚕️ Seguro de Saúde

🧬 Biotecnologia

Healthcare • Healthcare Insurance • Biotechnology

A Abbott é uma empresa global de saúde comprometida em avançar tecnologias médicas e melhorar a vida das pessoas em todo o mundo. Oferece um amplo portfólio de produtos líderes em diagnósticos, dispositivos médicos, nutrição e medicamentos genéricos de marca. Inovações da Abbott, como os sistemas de monitoramento de glicose FreeStyle Libre e os testes rápidos de antígeno BinaxNOW, estão transformando o manejo do diabetes e a resposta à COVID-19. Por meio de parcerias e iniciativas, a Abbott busca promover a equidade em saúde, ampliar o acesso aos cuidados de saúde e enfrentar desafios críticos, como a desnutrição e as doenças infecciosas. A Abbott também é dedicada à sustentabilidade e à responsabilidade social, trabalhando para tornar tecnologias que mudam vidas acessíveis e economicamente viáveis.

Descrição

• Lead the Field Clinical function for TMVR clinical studies • Develop programs, staffing plans, training programs, and budgets • Lead patient screening and selection for TMVR clinical studies using complex medical imaging and patient-specific analysis • Participate in developing and reviewing clinical research protocols, reports, and statistical analysis plans • Serve as a senior point of contact for Clinical Investigators and site research staff • Establish and monitor standardized operating models, policies, and performance metrics • Ensure compliance with FDA, ISO, MDR, and global regulatory requirements • Collaborate with Clinical Science to align with approved clinical strategies and evidence • Provide timely clinical data and program updates to stakeholders • Present study updates to senior leadership, investigators, and other stakeholders • Partner with Clinical Operations, Clinical Science, Quality, Regulatory, Marketing, Medical Affairs, Training, and Commercial functions • Provide strategic and operational leadership for field-based clinical teams supporting TMVR programs • Support safe, effective, and compliant clinical trial execution, training, case conduct, and patient outcomes

🎯 Requisitos

• Master's degree in Life Sciences, Engineering, Healthcare, or a related field with a minimum of 7 years of relevant experience; or Bachelor's degree in Life Sciences, Engineering, Healthcare, or a related field with a minimum of 9 years of relevant experience • Significant experience supporting complex structural heart clinical programs, including direct experience with Transcatheter Mitral Valve Replacement (TMVR) technologies, clinical studies, and procedures • Experience building, leading, and scaling field clinical teams supporting investigational medical device programs • Experience developing organizational capabilities, governance, and standardized operating processes • Strong understanding of structural heart disease, transcatheter valve therapies, advanced cardiac imaging, and anatomical patient screening and selection • Proven ability to maintain relationships with clinical investigators, physician leaders, and research sites • Ability to lead cross-functional clinical programs and ensure execution in regulated clinical trial environments • Strategic leadership, communication, and organizational management skills • Ability to influence senior leadership, develop managers, and lead geographically dispersed teams • Experience developing and managing budgets, staffing plans, and operational performance metrics • Knowledge of disease state and device usage • Knowledge of FDA, ISO, MDR, and global regulatory requirements

🏖️ Benefícios

• Career development with an international company • Free medical coverage through the Health Investment Plan (HIP) PPO medical plan for qualifying employees • Excellent retirement savings plan with a high employer contribution • Tuition reimbursement • Freedom 2 Save student debt program • FreeU education benefit toward a bachelor’s degree • Opportunity to grow and learn at a company recognized as a great place to work • Diversity, working mothers, female executives, and scientists workplace recognition

📊 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