Job Description
**Clinical Research Associate**
**Your responsibilities will include:**
+ Performing site selection, initiation, monitoring and close-out visits
+ Supporting the development of a subject recruitment plan
+ Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
+ Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
+ Collaborating with experts at study sites and with client representatives
**Qualifications:**
+ University degree in scientific discipline or health care
+ Minimum of **two-** **f** **our years of on-site monitoring experience** alternatively an equivalent combination of education, training and experience
+ Very good computer skills including MS O...
**Your responsibilities will include:**
+ Performing site selection, initiation, monitoring and close-out visits
+ Supporting the development of a subject recruitment plan
+ Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
+ Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
+ Collaborating with experts at study sites and with client representatives
**Qualifications:**
+ University degree in scientific discipline or health care
+ Minimum of **two-** **f** **our years of on-site monitoring experience** alternatively an equivalent combination of education, training and experience
+ Very good computer skills including MS O...
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