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Crosstrees Medical Work Values
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Daily Duties at Crosstrees Medical:
Monitors over 15 national clinical trial sites and 3 international sites. Writes protocols, consent forms, and protocol amendments for clinical trials. Trains study staff at various locations in how to participate in clinical trials through site qualification, initiation, and interim monitoring visits as well as at investigator and coordinator meetings. Assists in data collection and analysis. Performs close out site visits. Develops patient recruitment materials and processes to overcome enrollment obstacles at all sites. Serves as a liaison amongst site staff, analytical lab, sponsor management, translation services and CRO in China.
What they like about Crosstrees Medical:
Organizations with strong, centralized leadership are particularly attractive to you. You require a work environment with leadership that aggressively seeks to expand and grow the business and does so in a visible and decisive manner. In general you prefer to work in an environment in which there is a strong link between leadership, its actions, and a strong set of company-wide values.
Tags
professional, CRA, regulatory, research, clinical, medical writing
Information about Crosstrees Medical
Company Rank: Not Available
Average length of employment : 16 years
Average salary of employees: $53,000
These are some of the questions we asked our climbers about their experiences with Crosstrees Medical:
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| Were your performance expectations clearly communicated? | 0.0 |
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| Were you recognized for meeting or exceeding expectations? | 0.0 |
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| Did you feel like your personal contribution was important? | 0.0 |
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| Was your career path clearly outlined and discussed? | 0.0 |
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| I would recommend this as a place of employment. | 0.0 | |
| I believe in the purpose of this organization. | 0.0 | |
| I would work for this organization again. | 0.0 | |
| I feel employees are fairly compensated. | 0.0 |
