Research Assistant I - Clinical Research

CenExel•Los Angeles, CA

4d•$20 - $22•Onsite

About The Position

The Research Assistant I provides direct support to Clinical Research Coordinators in completing protocol-specific study goals while following ICH, GCP, study protocols, and site guidelines and policies. The role includes maintaining participant records, preparing study visits and materials, entering study data, assisting with assessments and monitoring visits, and communicating with participants and external parties. This is an indoor, office-based position with a Monday through Friday schedule from 8:00 a.m. to 4:30 p.m. Essential physical activities include sitting, typing, standing, and walking, with occasional lifting of up to 20 pounds. Reporting to work as scheduled is essential. CenExel Clinical Research conducts Phase I through Phase IV clinical trials across multiple specialty areas. The company describes its work environment as collaborative, with positive leadership and a focus on work-life balance.

Requirements

Interest in and knowledge of specific study indications.
Excellent computer skills and advanced knowledge of electronic equipment, including email, computers, fax machines, and copiers.
Organization and record-maintenance skills.
Ability to develop and maintain effective working relationships with supervisors and coworkers.
Strong personal initiative and attention to detail.
Ability to react calmly and effectively in emergency situations.
Ability to interpret, adapt, and apply guidelines and procedures.
Ability to communicate clearly orally and verbally.

Responsibilities

Create and maintain patient charts for assigned studies.
Prepare participant visits according to the Clinical Research Coordinator’s schedule, ensuring source documents, assessments, lab kits, and other visit materials are available and accurate.
File lab results, EKG results, and other communications in designated patient charts.
Maintain inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials.
Complete data entry and resolve queries for all CRFs within sponsor-specific timelines and established deadlines.
Assist Coordinators with assessments, including blood pressure measurement and urine collection.
Communicate with study participants, caregivers, third-party vendors, and laboratories as needed.
Assist Coordinators with scheduling, copying, faxing, and other clerical tasks.
Assist Coordinators in facilitating study monitoring visits.
Complete daily responsibilities delegated by the Clinical Research Coordinator relating to studies and participants.
Perform other assigned duties and responsibilities.