.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.**Discover Impactful Work**:Provides administrative and technical support to the Project Team. Coordinates responsibilities of project administration as applicable to the client contract under the direction of the assigned Project Lead.**Responsibilities**:- Reviews regulatory documents for accurate content.- Performs study investigator file reviews and logging of outstanding issues in project related tracking tools.- Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified.- Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD/TFS departments.- Assists Project Leads and Functional Leads with execution/facilitation of crucial tasks and results to expedite resolution and/or updates.- Provides tracking of training matrices, sop lists and completion adherence and requirements.- Attends high profile conference calls with Clients and provides sufficient response to inquiries.**Education**:- High/Secondary school diploma or equivalent and relevant formal academic/vocational qualification.- Bachelor's degree preferred.**Experience**:- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year).- In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.**Knowledge, Skills, Abilities**:- Ability to work in a team or independently as the need arises.- Good organizational skills and strong attention to detail, with proven track record to handle multiple tasks efficiently and effectively.- Proven ability to optimally analyze project-specific data/systems to ensure accuracy and efficiency.- Strong customer focus.- Flexibility to reprioritize workload to meet changing project timelines.- Good English language and grammar skills and proficient local language skills as needed- Good digital literacy, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems