Job Description
Looking for Clinical Research assistants/coordinators. Individuals must have an Associate or a Bachelor degree as well as a RN or LPN or MA certification. Candidates must have knowledge in multiple therapeutic areas. The purpose of the job is to coordinate phase I-IV in-patient or out-patient Clinical Research for investigational new drug studies. Candidates with prior Clinical Research Coordinator experience are encouraged to apply. Foreign Medical Graduates are also welcome to apply
Responsibilities:
• Involves in the patient screening and enrollment for the clinical studies
• Capable of performing phlebotomy
• Preparing and maintaining clinical trial source documents
• Conducting study visits, including vital signs, ECG, blood draw and processing
• Completing and ensuring the quality of case report forms
• Maintaining and dispensing drugs
• Preparing for site monitoring visits
• Preparing for site selection visits
• Maintaining documentation regarding all aspects of the study;
• Maintaining patient confidence and protects operations by keeping information confidential
• Participating Investigator's meetings
Skills/Qualifications:
• Associate or Four-year undergraduate degree or Foreign Medical Degree
• Prior CRC experience (preferred candidates)
• Phlebotomy
• RN or LPN or MA
• Good interpersonal and organizational skills
• Demonstrated strong communication, leadership and presentation skills
• Self-directed, proactive and timely in the management of the assignments
Benefits
- Medical, vision and dental insurance (After 90 day period)
- Flexible schedule
- Excellent work environment