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Job #03331

About our client Our client is a rapidly growing laboratory headquartered in Arizona that is focused on the development and commercialization in therapeutic areas such as oncology, dermatology, cardiology, osteoporosis and neurology. The company has premier investors, an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. Position Location Senior Clinical Project Manager Arizona Salary Highly competitive package, commensurate with experience Responsibilities 1) Handle all responsibilities related to the execution of a clinical development program from protocol design to the final clinical study report for one or several studies 2) Manage the process and people involved either as direct reports or though matrix reporting via the Clinical Indication Team 3) Coordinate all efforts for the trial both within and through a wide variety of vendors 4) Manage cross-functional project teams from the groups within clinical development to deliver a high-quality clinical trial or suite of clinical trials 5) Drive all aspects of project management process from initiation, planning, execution, control to closure 6) Plan and direct timelines, create project budgets as well as manage the cost according to the budget 7) Deliver the projects on time and within the budget 8) Create and maintain MS Project timelines for each project, using these timelines to track and manage project progress 9) Manage and coordinate all vendors involved in the clinical trials, e.g. central lab, CROs, including managing the RFP processes for each 10) Create project plans for each project Requirements 1) MS in Life Sciences or a related field 2) 10+ years of clinical research or related experience 3) 5+ years of experience in clinical project management 4) Experience in a key CRO/pharmaceutical operational function (e.g., data management, clinical operations, laboratory and pre-clinical) 5) Experience in oncology, osteoporosis, neurology and diabetes 6) Previous working experience in companies such as Covance, Genzyme, Merck, etc. 7) Phase II – IV management experience preferred 8) Experience in resource and budget/financial management 9) Knowledge of clinical study guidelines (FDA, ICH and GCP) 10) In-depth understanding of the clinical trials process 11) Excellent communication (written and oral), client management and IT (MS Office) skills 12) Individual with verifiable job stability (not a job hopper) and detail-oriented