.Sr Project Mgr Fsp | myGwork – LGBTQ+ Business Community | Portugal This inclusive employer is a member of myGwork – the largest global platform for the LGBTQ+ business community. Job Description 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. 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 This role will be embedded within a client-dedicated team. You will work alongside the client's own experienced personnel, as well as PPD colleagues to deliver innovative clinical support. Discover Impactful Work The Study Manager has global responsibility for one or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studies. Provides quality oversight to the Contract Research Organization (CRO) and of the CRO deliverables related to study execution. Leads and coordinates the execution of a clinical trial from Study start-up through Database close and inspection readiness to ensure timely delivery of quality study data. Study Managers may also input to and support compilation of sections to Clinical Study Reports. Will provide leadership to the teams in the setting of realistic recruitment targets and delivery milestones as the single point of accountability for detailed study start-up and monitoring plans and for delivery to the agreed plans. Works with functional lines and directly with CRO line functions to resolve or triage site level issues. Will drive decision making and work closely with the Clinical Project Manager to provide input to operational strategy. For studies where more than one Study Manager is assigned, may be required to act as 'lead' study manager, and will coordinate activities of the other Study Managers assigned. A Day In The Life Accountable for the development of realistic detailed study startup and monitoring plans as well as study delivery. Accountable for conducting country level feasibility in collaboration with Global Clinical Trial Execution and CROs, reviewing Pre-trial Assessment outputs, approving sites, and assessing site activation plans. Leads study risk planning process in context of site and subject. Coordinate study/protocol training & investigator meetings. Develops and provides key inputs to Clinical Trial Budget. Leads inspection readiness activities related to study management and site readiness. May produce or review model Informed Consent Document (ICD) and study/country/site level ICD, as appropriate
