Clinical Research Coordinator

Company Description

Arch Clinical Trials is guided by a commitment to innovation, integrity, and stewardship in clinical research. The organization focuses on advancing patient care through thoughtfully designed and executed clinical trials. A collaborative expert team works closely with strategic partners to bring high‑quality research solutions to sponsors and sites. Arch Clinical Trials offers a mission‑driven environment where professionals can contribute to meaningful improvements in healthcare and patient outcomes.

The Clinical Research Coordinator is a full‑time, on‑site role based in St Louis, MO. This position is responsible for coordinating and managing clinical trial activities, including participant screening, enrollment, and scheduling study visits. The coordinator will obtain and document informed consent, ensure adherence to study protocols, and maintain accurate, timely source documentation and case report forms. Daily tasks include managing regulatory binders, preparing study materials, communicating with investigators and sponsors, and tracking study timelines and milestones.

The role also involves monitoring participant safety, reporting adverse events, and supporting quality assurance processes to maintain compliance with regulatory and ethical standards.

• Candidates should possess strong knowledge of clinical research processes, including Research and Clinical Research Experience.
• Candidates should possess skills in participant rights and safety, including Informed Consent and ethical research practices.
• Candidates should possess expertise in study design and operations, including understanding of Protocol and Clinical Trials.
• Candidates should possess attention to detail, organizational skills, and the ability to manage multiple studies or tasks simultaneously.
• Candidates should possess effective written and verbal communication skills for interaction with participants, investigators, and sponsor representatives.
• Candidates should possess proficiency with electronic data capture systems and standard office software.
• Relevant experience in a clinical research setting and familiarity with GCP and regulatory guidelines is highly beneficial.
• A bachelor’s degree in a health‑related, scientific, or equivalent field is preferred; certification as a Clinical Research Coordinator is a plus.