Research Assistant I - Clinical Research

CenExel•Sherman Oaks, CA

2d•Onsite

About The Position

The Research Assistant I provides direct support to Clinical Research Coordinators in completing protocol-specific study goals while adhering to ICH, GCP, study protocols, and site guidelines and policies. The role supports participant visits, study documentation, data entry, supply management, communications, and monitoring visits. The position is based in an indoor office environment and is scheduled Monday through Friday, 8:00 a.m. to 4:30 p.m. The hourly pay range is $20.00–$21.50, depending on education, experience, and skillset. CenExel’s research sites conduct Phase I to Phase IV clinical trials across specialties including Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. CenExel describes its work environment as promoting teamwork, positive leadership, and work-life balance. Full-time employees are eligible for a benefits package after 30 days of employment.

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.
Ability to report to work as scheduled.

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 laboratory 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 case report forms (CRFs) according to sponsor-specific timelines and deadlines established in contracts or other communications.
Assist Coordinators with assessments, including blood pressure measurements 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.
Help Coordinators facilitate study monitoring visits.
Complete daily responsibilities delegated by the Clinical Research Coordinator related to studies and/or participants.
Perform other duties and responsibilities as assigned.