Project Manager I - Inhalation Lab

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting Job Description Program Manager I - (Pharma - Inhalation) Onsite role 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. Location/Division Specific Information Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. Discover Impactful Work: As an Program Manager I within our GMP analytical testing facility you will collaborate with multiple areas including clients, laboratory staff and sample management in the coordination of project setup, maintenance and closure of lab projects. This position is specifically for our Inhalations testing team. A day in the Life: Acts as the primary coordinator for the receipt and log-in of samples and standards Manages shipment requests Manages sample and standard workflows, including check-outs, shipping, relog and disposal activities to support laboratory analysis  Tracks project progress, within assigned client team and associated support teams, provides status updates  Initiates project set up process Manages reagent documents for client and team, including Certificates of Analysis (CofAs) and Safety Data Sheets (SDSs) Coordinates and tracks the completion of internal lab-based projects, including facility audits and incident reports Manages client communication related to sample and standard processes  Supports the client relationship manager with daily progress updates to ensure project completion Manages timelines; identifies and escalates risks as necessary Attends internal meetings Education and Experience:   Bachelor's degree or equivalent and relevant formal academic / vocational qualification  1- 2 years experience in sample management, lab analysis, project management/coordination in lab environment (or similar) Knowledge, Skills and Abilities: Good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines  Effective project management and organizational skills  Good computer skills  General knowledge of clinical trial processes and programs  Strong attention to detail and problem solving skills  Good written and verbal communication skills  Ability to effectively conduct oral presentations  Demonstrated experience in identification and resolution of technical problems in a professional environment  Ability to maintain a high degree of confidentiality with clinical teams  Ability to attain, maintain and apply a working knowledge of applicable procedural documents  Demonstrated positive attitude, enthusiasm toward work, and the ability to work well with others  Physical Requirements / Work Environment Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: Able to communicate, receive, and