Chear Center LLC - International Medical Graduate/ Research Coordinator
This individual will be responsible for conducting and managing subject research visits at clinic by following protocols and Standard Operating Procedures (SOPs). Responsibilities include:
Conduct multiple clinical trial research subject visits by closely following the trial specific protocol in accordance with GCP and FDA guidelines.
Coordinate the day-to-day research activities at the clinic under the supervision of Principal Investigator (Licensed MD).
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.
Recruits and interviews prospective subjects for clinical studies. Familiarizes potential subjects with the details of the study through phone contacts and personal interviews.
Ensures that the informed consent process has occurred, is properly documented and filed as required.
Recognizes AEs (adverse events) and SAEs (serious adverse events) and promptly notifies appropriate parties; e.g. Principal Investigator, Study Sponsor, and IRB.
May complete basic clinical procedures such as phlebotomy , ECGs, pulmonary function tests and obtaining blood pressure.
Job Types: Full-time, Part-time
IMG/FMG (license not required): 1 year (Preferred)
Apply on Indeed: