Project Manager

🕒 Agosto 7

🐎 Kentucky – Remoto

🐎 Kentucky – Remote

⏰ Tempo Integral

🟢 Júnior

🟡 Pleno

👷‍♀️ Gerente de Projetos

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Thermo Fisher Scientific

SiteLinkedInTodas as Vagas

10.000+ funcionários

Fundada em 1956

🏥 Saúde

📦 Logística

🏭 Manufatura

Healthcare • Logistics • Manufacturing

A Thermo Fisher Scientific é a líder mundial em servir à ciência, com receita anual de mais de US$ 40 bilhões. Sua missão é capacitar os clientes a tornar o mundo mais saudável, limpo e seguro, apoiando a pesquisa em ciências da vida, solucionando desafios analíticos complexos, aumentando a produtividade dos laboratórios e melhorando a saúde dos pacientes por meio de diagnósticos e do desenvolvimento de terapias que transformam vidas. Com uma equipe global, oferece tecnologias inovadoras e serviços farmacêuticos por meio de marcas como Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon e PPD.

Descrição

• Lead and coordinate central laboratory activities across clinical trial programs • Monitor and manage designated clinical trial protocols in Global Central Labs • Ensure overall project performance and client satisfaction throughout assigned trial lifecycles • Provide internal consulting on project management issues and identify process and efficiency improvements • Act as chief liaison to sponsors, operational personnel, internal departments, external vendors, and stakeholders • Oversee and coordinate study initiation • Review, interpret, translate, and program study protocols into complete and accurate databases • Facilitate technical and clinical laboratory information flow to stakeholders • Prepare study specification documents according to budgets and contracts • Maintain updated study master files with version controls • Ensure sponsor authorization, document sign-off, and contract completion before service delivery • Assure compliance with FDA, Good Clinical Practice, PPD SOPs, IATA, and biological-specimen transport regulations • Coordinate protocol amendment reviews and obtain cross-functional commitment to resolve gaps and issues • Educate investigator sites through protocol-specific laboratory procedure presentations and demonstrations • Manage day-to-day clinical trial activities, resolve issues, and answer queries • Consult with IT and data management groups on software and functionality design, validation, and implementation • Support RFP feasibility assessments and draft proposal responses • Guide, train, and mentor Project Managers and Set-up Administrators • Author, review, revise, and implement procedural documents • Serve as backup for the Associate Director PM when needed

🎯 Requisitos

• Bachelor’s degree or equivalent and relevant formal academic/vocational qualification • Previous experience providing the knowledge, skills, and abilities to perform the job, comparable to 2+ years, or equivalent combination of education, training, and experience • Strong verbal, written, and presentation skills • Superior time management, planning, and organizational skills • Competence with computers and enterprise applications, including office productivity applications • Ability to program the IT system according to protocol requirements • Proven analytical skills • Demonstrated compliance with procedures and policies • Ability to perform multiple tasks effectively in a stressful environment • Extensive knowledge and experience in project management in a Global Central Lab environment • Strong client relationship management skills • Ability to work effectively with multi-level teams • Ability to communicate, receive, and understand information and ideas with diverse groups • Ability to work upright and stationary for typical working hours • Ability to use and learn standard office equipment and technology proficiently • Ability to perform successfully under pressure while prioritizing and handling multiple projects or activities • May require travel • Must be legally authorized to work in the United States without sponsorship • Must pass a comprehensive background check, including drug screening

🏖️ Benefícios

• Fully remote work arrangement • Opportunity to collaborate with industry-leading experts • Contribution to groundbreaking clinical research • Career growth within an environment valuing innovation, accountability, and continuous development • Reasonable accommodation for applicants with disabilities • Equal employment opportunity and accessibility support