Clinical Research Assistant

Description

• Assist Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Assist Coordinators in assessments, including but not limited to blood pressure and urine collection.
• Communicate with study participants, caregivers, third-party vendors, and laboratories as needed.
• Create and maintain patient charts for all assigned studies.
• Complete daily responsibilities delegated by the Clinical Research Coordinator as they pertain to the study and/or participants.
• Assist with enrollment logs and other study-related documentation as needed.
• Prepare participant visits based on the Clinical Research Coordinator's schedule, ensuring all source documents, assessments, lab kits, and other visit materials are available and accurate.
• Aid Coordinators in the facilitation of study monitoring visits.
• 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.
• Complete data entry and query resolution for all Case Report Forms (CRFs) in a timely manner, based on sponsor-specific timelines and deadlines.
• Serve as the Clinical Research Coordinator's right hand in various tasks, including seeing patients and preparing lab kits and patient binders.

Requirements

• Ability to develop and maintain effective working relationships with supervisors and coworkers
• Ability to thrive in a fast-paced environment and multitask effectively.
• Ability to interpret, adapt, and apply guidelines and procedures
• Strong personal initiative and attention to detail
• Excellent computer skills and advanced knowledge of electronic equipment
• Proficiency in Microsoft Word and Excel.
• Bilingual in Spanish
• Bachelors degree in Biology, Psychology, or related
• Strong interpersonal skills and ability to communicate clearly both orally and verbally.
• Ability to react calmly and effectively in emergency situations
• Interest in and knowledge of specific study indications
• Skilled in organization and record maintenance

Benefits

Training + Development

Interview process

Visa Sponsorship

Security clearance