Clinical Research Monitoring (CRA)

Company Description Trialmed is a trusted clinical trial partner for patients, trial volunteers, and sponsors/CROs, integrating clinical research as a care option within the health care journey. The organization delivers patient-centered experiences through welcoming clinics, intuitive digital tools, and a strong commitment to quality. Trialmed’s extensive access to patients in its operating geographies supports reliable enrollment outcomes that meet or exceed sponsor expectations. Home Health Services provide flexible options for clinical trial visits at locations such as the patient’s home, office, or school. Trialmed offers scalable clinical trial solutions and a best-in-class site network from Phase I–IV, making it a destination of choice for patients and healthy volunteers.

Role Description This is a full-time, on-site Clinical Research Associate role based in Sandy Springs, GA. The Clinical Research Associate will support Clinical Research Coordinators to conduct clinical trials at assigned sites, ensuring adherence to study protocols, regulatory requirements, and Trialmed’s quality standards. Day-to-day responsibilities include monitoring patient safety, reviewing source documents and case report forms, verifying data accuracy, and supporting site staff with study procedures and documentation. The Clinical Research Associate will collaborate with clinical operations, investigators, and sponsors to address queries, resolve issues, and contribute to efficient, patient-centered trial execution.

Strong foundation in clinical trial protocols and their practical application in patient-focused research.

Experience working as a Clinical Research Associate or in a similar clinical research role.

Knowledge of clinical trials processes and regulatory frameworks, including GCP and ICH guidelines.

Background in research and clinical operations, with the ability to manage multiple studies or sites.

Bachelor’s degree in life sciences, nursing, pharmacy, or a related health/clinical field (advanced degree a plus).

Excellent attention to detail, documentation skills, and ability to interpret medical and scientific information.

Strong communication and interpersonal skills for working with patients, site staff, and sponsors.

Proficiency with electronic data capture systems and standard office software; comfort with digital health tools.

Ability to work on-site in Sandy Springs, GA, with occasional travel to local or regional study locations if required.

Prior experience in early-phase trials or multi-site clinical studies is beneficial.

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