Research Assistant

CenExel•Decatur, GA

13d•Onsite

About The Position

The Research Assistant I provides direct support to Clinical Research Coordinators, with moderate oversight, to complete protocol-specific study goals. The role requires strict adherence to ICH, GCP, study protocols, and site guidelines and policies. Work is performed onsite in an indoor office environment and includes sitting, typing, standing, and walking. The position is lightly active, with occasional lifting of up to 20 pounds and/or pushing carts up to 50 pounds. Reporting to work as scheduled is essential. CenExel is a nationwide clinical research site and patient network serving the life sciences industry. Its 18 science-led Centers of Excellence focus on CNS and early-phase studies, providing medical and scientific support for clinical trial design and execution.

Requirements

High school graduate or equivalent.
Excellent computer skills and advanced knowledge of electronic equipment, such as email, computers, fax machines, and copiers.
Skilled in organization and record maintenance.
Skilled in developing and maintaining 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, with occasional lifting of up to 20 pounds and/or pushing carts up to 50 pounds.
Must report to work as scheduled.

Responsibilities

Create and maintain patient charts for assigned studies.
Prepare participant visits according to Clinical Research Coordinators’ schedules, 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 CRFs within sponsor-specific timelines and deadlines established in contracts or other communications.
Conduct 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 studies and/or participants.
Assume other assigned duties and responsibilities.