Assistant Clinical Research Coordinator I

ALLIANCE CLINICAL LLC•Dallas, TX

12h

About The Position

This position is a full-time temporary position to fill in for maternity leave until mid-September and will be a full time temporary position, but could be extended based on company needs. The Assistant Clinical Research Coordinator I plays a vital role in supporting the planning, implementation, and management of clinical research studies within healthcare settings. This position ensures that clinical trials are conducted in compliance with regulatory requirements, institutional policies, and study protocols to protect participant safety and data integrity. The role involves close collaboration with principal investigators, research staff, and participants to facilitate smooth study operations and accurate data collection. The Assistant Clinical Research Coordinator I contributes to the preparation of study documentation, participant recruitment, and monitoring of study progress. Ultimately, this position supports the advancement of medical knowledge and patient care through rigorous and ethical clinical research practices.

Requirements

High school diploma or equivalent required; Associate’s degree or higher in a health-related field preferred.
Basic knowledge of clinical research principles and terminology.
Familiarity with medical terminology and healthcare environments.
Strong organizational skills and attention to detail.
Ability to communicate clearly and professionally with diverse populations.

Nice To Haves

Experience working in clinical research or healthcare settings.
Certification as a Clinical Research Coordinator (e.g., CCRC) or willingness to obtain certification.
Proficiency with electronic data capture systems and clinical trial management software.
Knowledge of regulatory requirements such as Good Clinical Practice (GCP) and HIPAA.
Experience with participant recruitment and informed consent processes.

Responsibilities

Assist in the coordination and execution of clinical research protocols under the supervision of senior research staff.
Recruit, screen, and enroll study participants according to protocol criteria and ethical guidelines.
Collect, record, and maintain accurate study data and documentation in compliance with regulatory standards.
Schedule and coordinate study visits, procedures, and follow-ups with participants and clinical teams.
Communicate effectively with study participants to provide information, answer questions, and ensure adherence to study requirements.
Monitor study progress and report any adverse events or protocol deviations to the research team.
Support the preparation and submission of regulatory documents and assist with audits and inspections.