Clinical Research Associate Jobs in Georgia, United States

Senior Clinical Research Associate with 2+ years on‑site monitoring experience. Conduct site monitoring, recruitment tracking, protocol training, and regulatory submissions.

<p style="text-align:left"><b>Job Description</b></p><p style="text-align:inherit"></p><p><b><u>CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS</u>: ALABAMA, GEORGIA, COLORADO, MASSACHUSETTS, MICHIGAN, MARYLAND, PENNSYLVANIA</b></p><p></p><p>The role is accountable for performance and compliance for assigned protocols and sites in a country.</p><p></p><p>Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company

Clinical Research team at Merck conducts oncology trials across the US. The Clinical Research Associate manages site relationships, ensures protocol compliance, performs remote and on‑site monitoring, and collaborates with cross‑functional groups to drive study performance. Remote work, candidates must reside in listed states, travel 65‑75% of time, 2‑3 days/week on site.

Clinical Research Associate I – Thermo Fisher Scientific, part of the global clinical operations team that supports pharmaceutical and biotech trials. The role conducts remote and on‑site monitoring visits, ensures protocol compliance, manages documentation, and collaborates with investigative sites to maintain data integrity.

Clinical Research Quality Control team at CenExel ensures the accuracy, consistency, and integrity of clinical trial documentation across its Centers of Excellence. The QC Associate reviews consent forms, case report forms, and TMF documents, identifies discrepancies, and collaborates with clinical operations, data management, and regulatory teams to maintain GCP and ICH compliance.

Clinical Operations at Worldwide Clinical Trials, a global CRO, drives clinical research across therapeutic areas. The Senior Clinical Research Associate, Rare CNS, manages site activities, conducts study initiation visits, and ensures regulatory compliance while supporting data collection and safety reporting.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate, Psychiatry, manages site activities, conducts study initiation visits, and ensures regulatory compliance while supporting data collection and safety reporting.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate manages site activities for rare CNS studies, conducts initiation visits, ensures regulatory compliance, and supports contract and budget negotiations.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas, including rare CNS diseases. The Senior Clinical Research Associate manages site activities from start-up to closeout, conducts initiation visits, ensures regulatory compliance, and supports data collection remotely.

Clinical Operations team at Worldwide Clinical Trials drives multi‑therapeutic clinical studies, including oncology, by managing site activities and ensuring regulatory compliance. The Senior Clinical Research Associate oversees site start‑up, conducts study initiation visits, trains sites, monitors safety and data, and closes studies, collaborating remotely with sites across the Southeast and Mid‑Atlantic.

Thermo Fisher Scientific Clinical Research team conducts multi‑therapeutic clinical trials across the US Southeast and West regions. The Clinical Research Associate II coordinates remote and on‑site monitoring, ensures protocol compliance, manages documentation, and supports site relationships.

Thermo Fisher Scientific Clinical Research team advances global health by delivering high‑quality clinical trials. The Senior Clinical Research Associate I monitors sites, conducts remote and on‑site visits, ensures protocol compliance, and manages data quality using risk‑based monitoring.

Clinical Research team at Thermo Fisher Scientific advances innovative therapies worldwide. The Clinical Research Associate II independently manages trial sites, conducts on‑site and remote monitoring, ensures protocol compliance and data quality, and collaborates with investigators and cross‑functional teams.

Join a global clinical research organization that has supported the top 50 pharmaceutical companies and 750+ biotechs across 2,700 trials in 100+ countries. As an Assistant Clinical Research Associate, you will perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead, providing support with site preparedness, logistical support to the monitoring process, and assisting with site management and remote monitoring tasks per SOPs and regulatory guidelines.

Join Thermo Fisher Scientific as a Senior Clinical Research Associate supporting top pharmaceutical and biotech clients. You will conduct remote and on-site monitoring to ensure protocol compliance, data accuracy, and regulatory adherence across oncology trials.

FSP team at Covance seeks Senior Clinical Research Associate 2 to lead monitoring of in‑vitro diagnostics trials across the US. The role conducts site monitoring, data verification, SAE reporting and supports site staff training while ensuring protocol compliance. Remote work from any US location with 50‑60% overnight travel required.

The Clinical Research Coordinator II at the Hope Clinic of the Emory Vaccine Center supports clinical and translational research in infectious diseases, vaccines, treatment, and prevention. Day-to-day, the role manages research databases and study documents, interfaces with and consents participants, supervises specimen collection and processing, ensures protocol compliance, prepares regulatory submissions, and may perform phlebotomy or diagnostics with appropriate credentialing.

The Clinical Research Coordinator II at the Hope Clinic of the Emory Vaccine Center supports the clinic's mission to conduct human research studies and clinical trials for infectious diseases of public health importance. Day-to-day, the role manages research project databases, develops study documents, interfaces with and consents participants, supervises specimen collection, ensures protocol compliance, prepares regulatory submissions, and may perform phlebotomy or diagnostics with appropriate

The Clinical Research Coordinator I supports the Children's Clinical and Translational Discovery Core (CTDC) within Emory University's School of Medicine - Pediatrics, Innovation Research. The role handles administrative and laboratory activities for clinical trials, including data entry, specimen processing, and regulatory tracking, to support pediatric research.

Hope Clinic of the Emory Vaccine Center conducts human research studies and clinical trials in infectious disease vaccines, treatments, and prevention. The Clinical Research Coordinator III independently manages key aspects of large or multiple small trials, oversees data management, trains staff, and ensures regulatory compliance while interfacing with participants and sponsors.