Clinical Research Coordinator

ELEVATE CLINICAL RESEARCH, INC.•Houston, TX

14h

About The Position

The Clinical Research Coordinator (CRC) plays a pivotal role in the successful execution and management of clinical trials within healthcare settings. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory requirements and institutional policies. The CRC serves as a liaison between investigators, study sponsors, and participants, facilitating effective communication and smooth study progression. By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to advancing medical knowledge and improving patient care through the rigorous conduct of clinical research.

Requirements

Bachelor’s degree in a health-related field such as Nursing, Life Sciences, or Public Health.
At least 2 years of experience coordinating clinical research studies or trials.
Comprehensive knowledge of clinical trial processes, regulatory requirements, and ethical standards.
Familiarity with clinical research documentation, including informed consent forms and case report forms.
Strong organizational skills and attention to detail to manage multiple study activities simultaneously.

Nice To Haves

Certification as a Clinical Research Coordinator (e.g., ACRP-CRC or SOCRA).
Experience working with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
Advanced knowledge of FDA regulations and Institutional Review Board (IRB) processes.
Previous experience in patient recruitment and retention strategies for clinical studies.
Master’s degree in Clinical Research, Public Health, or a related discipline.

Responsibilities

Coordinate and oversee the daily operations of clinical trials, including patient recruitment, informed consent, and scheduling study visits.
Ensure compliance with all regulatory requirements, institutional policies, and Good Clinical Practice (GCP) guidelines throughout the study lifecycle.
Maintain accurate and up-to-date regulatory documents, case report forms, and study databases to support data integrity and audit readiness.
Monitor study progress and patient safety by conducting regular assessments and reporting adverse events to the appropriate parties.
Collaborate with investigators, sponsors, and multidisciplinary teams to facilitate effective communication and resolve study-related issues promptly.