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| Job #03476 |
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| About our client |
| Our Client is a research site based in Dallas TX that conducts Phase 1-IV trials in multiple therapeutic areas. With many years of experience worldwide, our Client is a leader for patient recruitment and retention for the clinical trial industry. Due to expansion, they are urgently looking to hire a CRA to help with site selection and feasibility and patient recruitment management. This is an exciting opportunity for the right candidate to take on a challenging role! |
| Position |
Location |
| Clinical Research Associate |
Dallas, TX |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Feasibility and patient recruitment management 2) Oversee site selection 3) Oversee the implementation of clinical studies, study monitoring and management as well as data management/reporting 4) Serve as an efficient and experienced liaison between the study site staff and the company 5) Prepare regulatory reports and clinical documents 6) Create study management tools 7) Coordinate data collection/reporting with other departments |
| Requirements |
1) RN or BS in Biological Sciences or a related field (or an equivalent combination of education and experience) 2) 2+ years of CRA experience in monitoring clinical trials (from qualification to closeout) 3) Patient recruitment experience 4) Willing to get involved in project management for recruitment and retention projects after training 5) Knowledge and understanding of FDA regulations and GCPs along with their practical implementation 6) Exceptional interpersonal, problem-solving and communication (written and oral) skills 7) Willingness to travel depending on assignment |

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