ELEVATE CLINICAL RESEARCH, INC.·Atascocita, Texas
The Clinical Research Coordinator manages the daily operations of clinical trials, including patient recruitment, scheduling, and informed consent. They ensure strict compliance with regulatory requirements and maintain accurate study documentation to support data integrity.
Elevate Clinical Research is a mission‑driven organization expanding access to high‑quality clinical trials across Texas, Louisiana, Illinois, Maryland, Kansas, South Dakota, Hawaii, and growing. We exist to bring research closer to the communities that need it most, delivering compassionate patient care, operational excellence, and trustworthy data that advances medicine.
At Elevate, your work has real impact. Every role contributes directly to improving health outcomes and bringing new therapies to life. We hire people who care deeply about patients, believe in doing things the right way, and want to grow with a company that’s expanding nationwide.
Join Elevate and help build a patient‑centered research network that’s changing what clinical trials can look like for communities across the country.
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.
Candidates must have a bachelor's degree in a health-related field and at least 2 years of experience coordinating clinical research studies. Knowledge of regulatory requirements, ethical standards, and clinical documentation is essential.
Market context
Clinical Research Coordinator positions in Texas are often competitive because employers look for candidates who can manage protocols, documentation, and participant communication while working within ICH/GCP standards. This role typically favors applicants with clinical research experience, strong organization, and clear communication, and benefits like medical, dental, vision, life insurance, and paid time off can make offers more attractive. Review the AI-summarized requirements and benefits here to save time, then tailor your application to highlight GCP knowledge and hands-on research coordination experience.