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| Job #02387 |
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| About our client |
| Our client is a reputable, mid-size CRO that is experiencing unprecedented growth. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. |
| Position |
Location |
| Lead Clinical Research Associate |
New Jersey |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Support the Project Manager with study activities 2) Liaise with CRAs and Sponsors to track study progress and milestones 3) Regulate quality standards 4) Resolve logistic and practical issues and promote the team-working environment 5) Develop a comprehensive knowledge of the study protocol and other relevant documentation 6) Organize and conduct investigator meetings 7) Research and resolve data queries 8) Interact with senior staff regarding objectives and status of clinical projects 9) Prepare reports and make presentations |
| Requirements |
1) Bachelor’s degree in a scientific discipline 2) 4+ years of clinical trial experience in the pharmaceutical or biotech industry, including both site management and CRA supervision 3) 4+ years of field monitoring experience 4) Experience in oncology/cardiology/rheumatology 5) 1+ years of experience in supervising CRAs 6) Ability to anticipate problems relating to projects and develop/implement solutions 7) Highly effective in setting/meeting personal short/long term goals to complete assignments 8) Solid leadership skills 9) Strong interpersonal written/oral communication skills 10) Willingness to travel |

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