Clinical Trial Project Manager

Innomed is a clinical-stage biotechnology company focused on the development of first-in-class and best-in-class cardiovascular and metabolic innovative therapies, leveraging proprietary drug delivery and translational platforms. The company is preparing for HK IPO, with active multi-regional clinical trials in China, the US, Canada and Australia. About the Role Fully remote; Full time; Full benefits; Need to travel; pay up to $140k The Clinical Trial Project Manager is responsible for the end-to-end operational execution and oversight of the US portion of global clinical trials. This role leads the cross-functional Local Study Team (LST) to ensure trial delivery in alignment with the global program strategy. Key responsibilities include managing study budgets, vendor oversight, and site lifecycle activities (identification, onboarding, training, and oversight). The Project Manager drives quality and compliance by authoring and maintaining key study documents (e.g., monitoring plans), reviewing site trip reports, and providing direct training and oversight to CRAs, CTMs, and IH-CRAs. Additionally, this role supports country-level operational planning, communicates study status and timelines to global stakeholders (e.g., GCM, CST/TMT, DOM), and ensures accurate system updates to drive successful trial execution within the assigned region. Responsibilities Responsible for running the US portion of global trials, working with cross functional teams. Providing budget, and vendor oversite. Providing Site oversite, site training, Onboarding, Identification – selection support. Responsible for reviewing trip reports. Monitoring plan: Witten or contributed, updated, and made changes. Responsible for cross-functional team oversite and training for CRA’s, CTM’s, IH-CRA’s. Planning, management, and oversight of clinical study execution in accordance with the global program strategy, through leadership of the cross-functional Local Study Team (LST). Supports country-level operational planning and accountable for site selection within assigned country/-ies. Contributes and develops to program/study-specific materials – e.g., monitoring plan, study specific training documents. Supports and contributions to Clinical Study Teams (CSTs) / Trial Management Teams (TMTs) as applicable, agenda driven, present at meetings. Communicates country status (including timelines and deliverables) to key stakeholders (e.g., Global Clinical Managers [GCM], Program Managers, CST or TMT, Development Operations Manager [DOM] etc) with oversight as required and ensures updates to relevant systems. Qualifications Minimum 3 years’ experience running local/regional/global trials in a CRO, Pharmaceutical or Biotechnology environment. #J-18808-Ljbffr