Job Features
| Roles and Responsibilities | Responsible for assisting with the selection, initiation, regular monitoring and closeout of investigative sites. Requires flexibility, excellent interpersonal skills, previous industry experience, and the ability to work well with all levels of staff, as well as outside clients and vendors. Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data is a must. Sensitivity to confidential matters is required. |
| Education | Bachelors Degree of higher |
| Qualifications | 3+ years of relevant experience as a Clinical Research Associate |
| Preferred Experience | Medical Device and/or Diagnostic Trials, Detail Oriented, Excellent Communication Skills |
| Job Type | Full Time |
| Salary | Competitive, DOE |
| Benefits | Flexible Schedule, Health Insurance, Employer 401(k) Match |
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