Research Assistant/Medical Assistant

CenExel•Atlanta, GA

10d

About The Position

The Research Assistant/Medical Assistant 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 clinical research activities across CenExel’s Phase I to Phase IV studies and helps maintain accurate participant records, prepare study visits, manage study supplies, enter data, and assist with participant assessments and communications. Compensation is $20–$21 per hour, depending on experience, education, and skillset. CenExel’s research sites conduct studies in specialties including Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. The company describes a team-oriented work environment that promotes 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.
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, orally and verbally.
Ability to report to work as scheduled.

Nice To Haves

Phlebotomy experience.

Responsibilities

Create and maintain patient charts for assigned studies.
Prepare participant visits using the Clinical Research Coordinator’s schedule, ensuring source documents, assessments, lab kits, and other 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 according to sponsor 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 relating to the study and/or participants.
Perform other duties and responsibilities as assigned.