Focused on obtaining a position as a Clinical Research Associate. Detail oriented with the ability to plan organize coordinate and manage projects according to priorities. Ongoing and consistent promotion of team work efforts. Excellent Communication and Interpersonal skills. Excellent oral and written communication skills with the ability to communicate effectively with medical personnel. Quick learner with the ability to assimilate job requirements concepts methods and technologies. Proven flexibility and adaptability. CRC professional with experience in all areas of clinical research and site management including site identification/evaluation site initiation interim monitoring visits site closeout knowledge of ICH GCP guidelines serious adverse event reporting IRB protocol submissions and on-going regulatory document review. Willing to travel 40-80%

Highlights:

• Documentation
• Management
• Cardiovascular
• Cardiology
• Clinical Research
• Distribution
• Good Clinical Practices
• Research