Find Jobs
Find Jobs Near You – Available Work in Your Location
Find & Apply For Clinical Research Coordinator Jobs in Sugar Land, Texas
Browse jobs from a variety of sources below, sorted with the most recently published, nearest to the top. Click the title to view more information and apply online.
Skip to job details
Now viewing: Assistant Clinical Research Coordinator
TN
Tricoastal Narcolepsy and Sleep Disorders Center
Assistant Clinical Research Coordinator
Entry-Level JobVerifiedNo experience needed
Job Description
Assistant Clinical Research Coordinator Tricoastal Narcolepsy and Sleep Disorders Center Sugar Land, TX Job Details Full-time | Contract 1 day ago Qualifications Records management Bachelor's degree Data management Attention to detail Quality audits Appointment scheduling Full Job Description We are seeking a dedicated and detail-oriented Assistant Clinical Research Coordinator to join our dynamic clinical research team. In this role, you will provide critical support to the clinical research staff, investigators, and study participants by assisting with the day-to-day coordination and administration of clinical trials. This position is ideal for individuals looking to build a rewarding career in clinical research, healthcare administration, or biomedical science. Key Responsibilities Assist Clinical Research Coordinator (CRC), Principal Investigator (PI), and Principal Sub-Investigator (Sub-I) with daily study operations and participant management. Help recruit, screen, and schedule prospective study participants in accordance with strict protocol inclusion/exclusion criteria. Assist in preparing study documentation, including regulatory binders, source documents, and participant recruitment materials. Maintain accurate, up-to-date study participant logs, case report forms (CRFs), and research records while ensuring strict data integrity and confidentiality. Collect, process, store, and ship biological specimens (blood, urine, etc.) under established laboratory safety and protocol guidelines. Help coordinate study-related visits, diagnostic tests, and laboratory appointments for participants. Liaise with hospital departments, laboratories, and external vendors to facilitate smooth study workflows. Prepare for and assist with internal quality control audits, sponsor monitoring visits, and regulatory inspections. Attend regular study team meetings, investigator meetings, and ongoing protocol training sessions.