Clinical Research Coordinator
Listed on 2026-01-02
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Healthcare
Clinical Research, Medical Science -
Research/Development
Clinical Research, Medical Science
Company Description
Pivotal Research Solutions, LLC (PRS) is a clinical research site based in Stonecrest, GA, dedicated to bridging the gap between research participants and the pharmaceutical industry. With expertise spanning areas such as hematology/oncology, cardiology, neurology, dermatology, urology, endocrinology, rheumatology, reproductive health, pulmonary health, rare diseases, and vaccine research, PRS stands at the forefront of clinical research. PRS conducts trials in diverse therapeutic areas, including pediatric and adult studies, and leverages extensive experience with specialized and complex research protocols.
PRS is committed to advancing medical knowledge and improving patient care through high-quality and ethical clinical research practices.
This is a 32-hour/wk on-site role in Stonecrest, GA, for a Clinical Research Coordinator. The Clinical Research Coordinator will oversee and coordinate clinical trials, ensure ethical and accurate implementation of research protocols, and manage informed consent processes with participants. Responsibilities include supporting patient recruitment, maintaining meticulous research documentation, and collaborating with healthcare providers to monitor participant progress and ensure compliance with clinical trial protocols.
Qualifications- Knowledge and proficiency in conducting informed consent processes, ensuring ethical coordination with study participants
- Demonstrated ability to interpret and implement clinical research protocols accurately
- Experience in clinical research and familiarity with clinical trials and related processes
- Strong organizational and communication skills, with attention to detail and adherence to regulatory compliance
- Ability to work on-site and collaborate with a multidisciplinary team in a dynamic clinical setting
- Bachelor's degree in a relevant scientific or healthcare-related field preferred
- Experience with electronic data capture systems and familiarity with FDA and GCP guidelines is a plus
- Ability to function in a team environment
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