Sarahi Monsalve

• Understand all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator.
• Assess eligibility of potential patients and oversee patient enrollment to ensure that informed consent is properly obtained and documented.
• Coordinate and conduct patient visits (drawing blood, collecting vital signs, performing ECGs, and processing specimens) and assure all procedures are conducted in compliance with the clinical trial protocol and Good Clinical Practice (GCP).
• Develop and maintain relationships with Sponsor and Contract Research Organization (CRO)
• Provide comprehensive training to clinical research coordinator, ensuring they are well-prepared to conduct study-related activities in compliance with protocol and regulatory requirements
• Involved in data management, regulatory coordination, and compliance monitoring

• Monitor patient’s health and vital signs and report updates to nurses and doctors.

• Assist with activities of daily living like bathing, feeding, walking, and grooming. • Aid in medical procedures performed by the nurses.

• Determine donor suitability by implementing different medical functions such as weight, temperature, blood pressure, pulse, hematocrit, and protein tests.

• Participate in the plasmapheresis procedure by performing venipunctures, collecting samples, and safely using plasma equipment.