
10,000+ employees
Founded 1956
đ„ Healthcare
đŠ Logistics
đ Manufacturing
Healthcare âą Logistics âą Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
đ„ 41 minutes ago
Where this job comes from
Posted on Thermo Fisher Scientific's careers page, not through a job board
First seen by Remote Rocketship 41 minutes ago

10,000+ employees
Founded 1956
đ„ Healthcare
đŠ Logistics
đ Manufacturing
Healthcare âą Logistics âą Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
âą Manage complex site operations and ensure compliance with regulatory standards âą Support site recruitment and training efforts âą Facilitate collaboration between trial sites and internal teams âą Oversee site activation for assigned projects within timelines and quality standards âą Coordinate information flow between PPD teams, clients, and functional departments âą Develop project implementation plans and guidelines using PPD tools âą Monitor and analyze project status, completion, and metrics for upper management âą Identify risks and provide contingency planning âą Manage financial and contractual aspects related to site activation âą Establish controls aligning project resources and expenses with budgets âą Administer feasibility, site contracts, and country-team coordination âą Manage assigned scope against timelines, costs, and quality âą Identify and evaluate issues affecting successful site activation and implement solutions âą Develop customer relationships aligned with assigned projects
âą Bachelor's degree or equivalent and relevant formal academic / vocational qualification âą Previous experience comparable to 5+ years âą An equivalency consisting of appropriate education, training and/or directly related experience may be considered âą Ability to work efficiently with cross-functional teams âą Knowledge of cross-functional project management principles âą Organizational and multitasking skills âą Attention to detail âą Ability to identify and remedy risks related to contractual deliverables âą Cross-cultural awareness and adaptability âą Comprehensive understanding of clinical research/development, medical and therapeutic areas, study phases, and medical terminology âą Ability to lead, liaise, and coordinate cross-functional project teams âą Comprehensive knowledge of clinical development guidelines and Directives âą Ability to access and use in-house and off-the-shelf computer software âą Ability to communicate and understand spoken and written information âą Regular and consistent attendance âą Ability to work under stress and multitask
âą Global team environment âą Collaboration and development opportunities âą Occasional travel to site locations, domestic and international
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