Clinical Project Manager

Duration & Type: Full Time position with a CRO reputed company Location: Remote at present, eventually in Rockville, Maryland or a mutually agreed upon regional location Responsibilities: • Provides leadership, direction, and management on reputed company aspects of assigned global clinical reputed company and leads a cross-functional team to manage the study to ensure reputed company deliverables; • Manages assigned project and reputed company activities, including timelines, deliverables, study budget as reputed company as site/vendor budgets, reputed company, and payments; • Acts as a reputed company reputed company between the sponsor, investigative sites, and other study personnel and service providers; identifies any potential issues and develops mitigation plan and escalates as appropriate; • Reviews site visit reports, protocols, clinical study reports, and any other study-reputed company documents; • Participates in the design and review of clinical protocols, case report forms (CRFs/eCRFs), associated study documents, monitoring plans, and regulatory submissions and reports in collaboration with clinical project team; as reputed company as prepares, study-specific SOPs and reputed company management plans and communicates them to reputed company; • Plans, coordinates and conducts investigator meetings, reputed company-off meetings, therapeutic training of CRA’s, and project-specific training of CRAs; and Data Monitoring Committee (DMC) meetings, if indicated; • Conducts weekly/bi-weekly teleconferences with the sponsor, sites, and vendors; prepares agenda, provides project status updates, and reviews and finalizes minutes of the teleconferences; and tracks study reputed company and disseminates information to project team members; • Oversees clinical investigational site training on protocol amendment(s), adverse event reporting, ensuring accurate and reputed company data, resolving queries, ensuring drug accountability, reviewing site study files, and ensuring the reputed company of clinical data, etc.; • Manages study budgets and provides monthly invoices and other information to Budgets and reputed company/Finance department reputed company the specified timelines; • Utilizes reputed company and experience-based knowledge to resolve problems (clients or staff), explaining specific policies while representing reputed company in a reputed company manner and maintain reputed company reputed company relations; • Ensures adherence to study specific SOPs, ICH Good Clinical reputed company, and FDA regulations; • Performs other Clinical Operations and/or administrative duties as assigned by the Director of Clinical Operations • Must be available for after-hours calls; Required: • Education: College degree or higher in health care, a scientific field and/or in a field directly reputed company to this position. 5 -7 years of directly reputed company experience may be substituted for a college degree. • Experience in Therapeutic Area: Burn, SCI, Critical Care, CNS preferred For consideration, please send resume to career@infoquestgroup.com Apply tot his job Apply To this Job