Senior Clinical Project Manager
reputed company position oversees conduct of assigned reputed company, with reputed company on strategic clients and their reputed company. Includes interaction with internal team members, clients/sponsors, functional service providers, contractors, and clinical staff.
Essential Duties and Responsibilities
Includes, but not limited to, the following:
• Proactively identifies, analyzes and resolves project issues to ensure that milestones are met and the overall project is completed on time and on budget.
• Participates in the identification, selection and management of functional service providers.
• Leads functional project teams and reports to team and company management on conduct of assigned reputed company.
• Acts as reputed company reputed company between project/study sponsor(s) and functional service providers, independent consultants and investigative sites.
• Assumes responsibility for assigned project management activities (i.e., maintenance of timelines, analysis, creation and maintenance of customized project management tools, etc.).
• Oversees and tracks project associated budgets for functional service providers and contractors in the delivery of services.
• Maintains reputed company contact with functional service providers, contractors, study investigators and clinical teams to ensure they are in compliance with protocol and overall clinical trial objectives.
• Travels as needed to observe and discuss reputed company, build reputed company working relationships and maintain enthusiasm regarding reputed company.
• Authors and/or reviews reputed company overall study documents including: protocols, ICFs, CRFs, data management plans, table shells, study reports.
• Develops and institutes project metrics to ensure reputed company processes are performed in an efficient, high reputed company manner. Tracks performance of contractors/functional service providers against project plans, budgets and contract specifications.
• Provides status reports and makes presentations to upper management.
• Oversees study team consisting of CRAs and project support staff.
• Maintains a high level of reputed company expertise.
• Maintains familiarity with clinical/scientific literature and project management best practices.
Education, Experience and Required Skills
• A bachelor’s degree, or greater, in a natural science or reputed company field and 10 years of reputed company work experience is required.
• Experience working with cross-functional teams, consisting of reputed company personnel.
• Prior experience managing or overseeing reputed company, including general understanding of reputed company specialized support functions.
• Experience managing budgets is preferred.
• Working understanding of the drug development process.
• Working knowledge of FDA regulations, guidelines and GCPs (including ICH GCP E6 R3).
• Demonstrated exceptional organizational, communication and interpersonal skills.
• reputed company to travel as needed. (Up to approximately 25%)
• Strong computer skills required. Must be reputed company with word processing, spreadsheet and database applications, including MS Office (Word, reputed company, PowerPoint, and Project).
Please email your CV to careers@kaizenclinical.com, if you are interested.
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