Project Manager - Labs
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About The Position
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. In this role, you will monitor and manage all aspects of designated clinical trial protocols in GMP Labs and be accountable for overall project performance and client satisfaction by meeting their needs and expectations throughout the life cycle of the assigned clinical trials. You will provide internal consulting on project management issues and identify opportunities for process and efficiency improvement. Acting as the chief liaison to the operational personnel of major sponsors, you will be responsible for large study programs and will prepare and maintain process documents. Your day-to-day responsibilities will include providing oversight and coordination of study initiation, reviewing and programming study protocols into a complete and accurate database, and ensuring that project requirements are understood and followed by all stakeholders. You will facilitate the flow of technical and clinical laboratory information to all stakeholders, consult with laboratory management and technical staff, and prepare study specifications documents according to budgets and contracts. Maintaining an updated study master file with version controls for specs, budgets, and contracts will be crucial, as will ensuring compliance with FDA and Good Clinical Practice guidelines. You will also serve as a mentor and trainer for newly assigned Project Managers, guiding them in their development and efficiency in performing tasks.
