Research Assistant/Medical Assistant

CenExel•Atlanta, GA

10d•$20 - $21•Onsite

About The Position

The Research Assistant/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. Responsibilities include preparing and maintaining study records and visit materials, supporting participant assessments and communications, and assisting with study data entry and administrative tasks. This position is in an indoor office environment and involves sitting, typing, standing, and walking. It is lightly active, with occasional lifting of up to 20 pounds. Reporting to work as scheduled is essential. Compensation is $20–$21 per hour, depending on experience, education, and skillset.

Requirements

Excellent computer skills and advanced knowledge of electronic equipment such as email, computers, fax machines, and copiers.
Strong organizational and record-maintenance skills.
Experience working with patients.
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, both orally and verbally.
Ability to meet the essential physical requirements of sitting, typing, standing, and walking, and occasional lifting of up to 20 pounds.
Ability to report to work as scheduled.

Nice To Haves

Interest in and knowledge of specific study indications.
Phlebotomy experience preferred.

Responsibilities

Create and maintain patient charts for assigned studies.
Prepare participant visits according to the Clinical Research Coordinator's schedule and ensure 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 all CRFs within sponsor-specific timelines and deadlines established in contracts or other communications.
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 CRC related to the study and/or participants.
Perform other duties and responsibilities as assigned.