Clinical Research Coordinator

Job Requirement: Clinical Research Coordinator (CRC) – Entry Level Job Title: Clinical Research Coordinator (CRC) – Entry Level Location: Texas, United States Job Type: Full-Time Experience: 0–3 Years (Freshers & Recent Graduates are encouraged to apply) Job Summary We are seeking a highly motivated and detail-oriented Entry‑Level Clinical Research Coordinator (CRC) to join our clinical research team in Texas. The candidate will support clinical trials by coordinating study activities, maintaining accurate documentation, ensuring regulatory compliance, and assisting investigators with patient‑related procedures. Key Responsibilities Assist in planning, coordinating, and managing clinical research studies. Recruit, screen, and schedule eligible study participants. Explain study procedures and assist with informed consent documentation. Collect and accurately maintain patient and clinical trial data. Maintain source documents, regulatory binders, and study records. Ensure compliance with study protocols, ICH‑GCP guidelines , FDA regulations, and institutional policies. Coordinate patient visits, laboratory samples, and study procedures. Communicate effectively with Principal Investigators (PIs), sponsors, and study participants. Report adverse events, protocol deviations, and study updates to the research team. Assist during sponsor visits, audits, and regulatory inspections. Required Qualifications Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, Biochemistry, Public Health, or a related healthcare field . Basic understanding of clinical research and clinical trial processes. Strong verbal and written communication skills. Excellent organizational and documentation skills. Proficiency in Microsoft Office (Word, Excel, PowerPoint). Ability to work independently and as part of a multidisciplinary team. Preferred Qualifications Clinical Research Certification (CRC/CCRC, GCP training) is a plus. Internship, academic project, or healthcare experience preferred but not mandatory. Knowledge of medical terminology and electronic data capture (EDC) systems is an advantage. Required Skills Time management Patient interaction and communication Data entry and documentation Problem‑solving skills Ability to maintain confidentiality and professionalism Competitive salary package Medical, dental, and vision insurance Paid time off (PTO) and holidays Clinical research training and mentorship Career growth opportunities within the clinical research industry #J-18808-Ljbffr