Clinical Research Coordinator II

Clinical Research Coordinator II Client: Major Clinical Research Client Duration: 9+ Months Contract Location: Katy TX Pay Rate: $26.17 - $29.08/ Hr on W2 Typical Hours 9:00 AM – 3:30 PM with a 30-minute lunch 9:00 AM – 4:00 PM with a 1-hour lunch Summary Seeking a Study Coordinator to support ongoing clinical studies in the United States. This role is responsible for completing all required documentation to capture study data as specified by the study protocol while ensuring participant safety, understanding, and cooperation throughout the study process. The position involves working closely with research site teams and internal departments while supporting the full site operations process, including recruitment, enrollment, participant retention, data entry, and query resolution. Candidates must have at least 1 year of previous experience as a Study Coordinator. Essential Functions Conduct clinical studies in accordance with FDA/GCP and ICH regulations and guidelines. Provide patient care while ensuring participant safety remains the top priority. Schedule participant visits within protocol windows while maximizing scheduling efficiency. Perform defined study activities, including informed consent, screening, and protocol procedures such as vital signs, pregnancy tests, height, weight, ECGs, and related activities. Record participant information and test results according to protocol requirements on required forms. Complete investigational product accountability logs and associated documentation when required. Report suspected non-compliance to appropriate site staff. Ensure IRB approval is obtained prior to study initiation and maintained throughout the study. Build positive relationships with participants to support retention. Attend site initiation meetings and other required meetings for protocol-related training. Conduct participant outreach, scheduling, booking confirmations, and follow-up calls as needed. Enter and maintain accurate information within sponsor systems, including case report forms and EDC systems, within required timelines. Gather and maintain source documents while ensuring participant files and notes remain current and accurate. Adhere to company policies, procedures, and standards. Assist with maintaining a clean and organized facility environment and proper disposal of waste according to established standards. Education and Experience Bachelor’s degree or equivalent relevant academic/vocational qualification in the clinical or medical field. Valid nursing license (RN, LVN, or LPN) required and must be registered with the applicable healthcare authority. Previous experience equivalent to 2+ years in a related clinical research role. Knowledge, Skills, and Abilities Solid understanding of the clinical research process, including GCP, SOPs, informed consent, and safety monitoring. Ability to work independently with strong attention to detail while handling sensitive and complex information. Strong analytical and problem-solving skills. Demonstrated ability to exercise discretion and sound judgment. Good decision-making, negotiation, and influencing skills. Strong communication skills; English fluency preferred. Strong organizational and interpersonal skills with the ability to work effectively in a team environment. Proficiency in basic computer applications. #J-18808-Ljbffr Radiant Systems Inc