Clinical Research Assistant (Must Live in Los Angeles and Speak Spanish)

Essential Responsibilities and Duties

• Create and maintain patient charts for all assigned studies.
• Prepare participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. File lab results, EKG results, and other communication in designated patient charts.
• Maintain inventory of study specific supplies including lab kits, assessments and participant facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
• Assist Coordinators in assessments, blood pressure, urine collection, draw labs.
• Communicate with study participants, caregivers, third party vendors and laboratories as needed.
• Assist Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aid Coordinators in the facilitation of study monitoring visits.
• Complete daily responsibilities delegated by CRC as they pertain to the study and/or participants.
• Assume other duties and responsibilities as assigned. Perform office/administrative tasks such as resupplying exam rooms, ordering office supplies, answering phone calls, etc.

Education/Experience/Skills

• High school graduate or equivalent.
• Bac
• Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
• Skilled in organization and record maintenance.
• Strong personal initiative and attention to detail.
• Ability to clearly communicate both orally and verbally.
• Prior experience in healthcare, research, or clinical settings is a plus.
• Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus.