Lead Clinical Research Coordinator
CurrentCreating and modifying source documentation to adhere to study protocol requirements. Organize, schedule, and mentor patients for study visits. Performing study related procedures: phlebotomy, EKGs, spirometry assessments, vitals signs, subcutaneous and intramuscular injections. Reviewing medical records and documenting accordingly per protocol. Collecting data from study visits and submitting data to pharmaceutical sponsors. Processing and packaging of laboratory assessments.