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| Job #02422 |
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| About our client |
| Our client is a publicly traded biopharmaceutical company headquartered in Washington that is dedicated to the development and commercialization of antibody-based therapeutics for the treatment of cancer. The company has 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 |
Washington |
| 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 the project management process from initiation, planning, execution, control and closure 6) Plan and direct timelines, create project budgets and manage cost to budgets 7) Deliver the projects on time and on budget 8) Work with functional areas on initiating, planning, executing, controlling, closing and resourcing clinical trial projects 9) Create and maintain MS Project timelines for each project, using these timelines to track and manage project progress 10) Create Project Plans for each project 11) Manage and coordinate all vendors involved in the clinical trials, e.g. central lab, CROs, including managing the RFP processes for each |
| Requirements |
1) Bachelor's degree, advanced degree (Master’s or Ph. D) preferred 2) 10+ years of pharmaceutical clinical development experience (at least 4 years of those as a PM) 3) NDA filing experience as well as international clinical trial development experience 4) Experience in both CRO and contract management 5) Oncology or hematology clinical trial experience preferred 6) Project Management Certification (PMP) a plus 7) International trial management experience preferred 8) Ability to negotiate and manage competing priorities across multiple functional areas |

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