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| Job #02765 |
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| About our client |
| Our client is a reputable, privately held CRO that is experiencing unprecedented growth. The company has an experienced management team, a very high customer-retention rate, industry low-employee turnover and a dedication to helping their staff maintain a strong work-life balance. This is a great opportunity for the right candidate! |
| Position |
Location |
| Clinical Research Associate (Home-Based) |
East Coast, USA |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Implement clinical studies, study monitoring, study management and data management/reporting 2) Liaise efficiently between study-site staff and company 3) Prepare regulatory reports and clinical documents 4) Create study management tools 5) Coordinate data collection/reporting with other departments 6) Assist with the development of junior staff 7) Participate in departmental programs |
| Requirements |
1) RN or BS in Biological Sciences or a related field (or 6+ years of experience in field monitoring) 2) Minimum 3 years of CRA experience in monitoring clinical trials from qualification to closeout 3) 3+ years of experience in field monitoring 4) In-depth knowledge of FDA regulations, GCPs and their practical implementation 5) Superb problem-solving skills 6) Proven record of job stability (multiple year at each tenure) 7) Excellent interpersonal and communication skills 8) Home office with a high-speed internet connection 9) Willingness to travel overnight – up to 65% |

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