Medical Assistant - Clinical Research

CenExel•Anaheim, CA

5d•$20 - $22•Onsite

About The Position

The Medical Assistant provides direct support to Clinical Research Coordinators in completing protocol-specific study goals. The role requires strict adherence to ICH, GCP, study protocols, and site guidelines and policies. CenExel’s research sites conduct Phase I through Phase IV clinical trials across specialty areas including Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. The position is full-time and scheduled from 7:00 pm to 3:30 pm, with weekends. The hourly pay range is $20.00–$21.50, depending on education, experience, and skillset.

Requirements

California Medical Assistant Certification.
Excellent computer skills and advanced knowledge of electronic equipment, such as 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 meet the essential physical requirements of sitting, typing, standing, and walking, with occasional lifting of up to 20 pounds.

Nice To Haves

Interest in and knowledge of specific study indications.

Responsibilities

Create and maintain patient charts for assigned studies.
Prepare participant visits based on 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 CRFs within sponsor-specific timelines and other 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 related to the study and/or participants.
Perform other assigned duties and responsibilities.