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| Job #03031 |
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| About our client |
| Our client, a world leading CRO, provides a broad range of services to the pharmaceutical, biotech and healthcare industries for the development and commercialization of various therapeutics. |
| Position |
Location |
| Clinical Project Manager |
West Coast, USA |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Manage single and full service clinical projects (both regional and global in scope) 2) Lead the cross-functional project teams including clinical operations, data management, biostatistics, medical writing and clinical QA 3) Ensure quality as well as on time and within budget deliverables for Phase II – IV clinical trials 4) Manage the clinical study timelines, deliverables and risks 5) Work with the client and Business Services to finalize the project budget and scope 6) Serve as primary contact with client to ensure appropriate communication 7) Participate in internal and external meetings 8) Manage project budget |
| Requirements |
1) BS in Life Sciences or a related field 2) 2+ years of experience in a project management environment 3) 5+ years of experience in clinical research or any other relevant experience 4) Experience in a key CRO/pharmaceutical operational function, e.g., data management, clinical operations, laboratory and pre-clinical 5) Experience in resource and budget/financial management 6) Superb Phase II – IV management experience preferred 7) Knowledge of clinical study guidelines, including FDA, ICH and GCP 8) Excellent client management skills 9) Good communication skills (written and verbal) 10) Excellent software skills including MS Excel, PowerPoint, and MS Project (or other similar Project Management tools) 11) Ability to firmly grasp the clinical trials process |

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