Position Requirements:
Minimum 5 years Experienced research to conduct multiple clinical trials
Coordinate research activities at the clinic under the supervision of Principal Investigator (Licensed MD) and Site director.
Review, extract and analyze data from medical charts for initial screening/identification of eligible subjects
Assess protocol inclusion/exclusion criteria and confirms eligibility of subjects.
Recruit and interviews prospective subjects for clinical studies
See patients and handle all patient visits for the various studies
Complete basic clinical procedures such as drawing blood, ECGs, pulmonary function tests and obtaining blood pressure
Experienced in study start up and regulatory
Able to manage a staff
Must have GCP and IATA certification
Should have experienced in different EDC formats
Should be hard Working
Meticulous/ detail oriented
Good with people
Must have 3 Reference work relate
ONLY QUALIFIED RESUMES WILL BE CONSIDERED
