NextCode Placement specializes in connecting skilled professionals with organizations across the technology, healthcare, and related industries. The company provides tailored career guidance and job-search support designed to align candidates's skills and career goals with relevant opportunities. NextCode Placement focuses on supporting candidates throughout their career journey by providing resources, professional guidance, and career-development services. Role Description The Clinical Research Associate (CRA) is a full-time, on-site position based in Texas, United States. The CRA will be responsible for monitoring clinical trial sites, ensuring compliance with study protocols, and supporting adherence to applicable regulatory and ethical standards. Key responsibilities include reviewing source documents and Case Report Forms (CRFs), verifying data accuracy and completeness, supporting site staff with clinical trial procedures, and documenting findings through monitoring reports. The CRA will collaborate with clinical operations teams and support site initiation, routine monitoring, and closeout activities. The role also involves identifying and helping resolve issues that may affect patient safety, protocol compliance, data integrity, or study timelines. Regular communication with investigators, clinical research coordinators, site personnel, and internal stakeholders will be required to ensure study quality and timely execution. Qualifications Bachelor's degree in Life Sciences, Nursing, Pharmacy, Biology, or a related field. Master's degree or advanced qualification in Clinical Research, Life Sciences, Pharmacy, Biotechnology, or a related discipline is a plus. Hands-on experience as a Clinical Research Associate (CRA) or in a closely related clinical research position. Strong understanding of clinical trial protocols, GCP, and applicable regulatory requirements. Knowledge of clinical trial processes, including site monitoring, documentation, source data verification, and data review. Experience with clinical operations, site management, and collaboration with cross-functional teams. Familiarity with Electronic Data Capture (EDC) systems and clinical trial management tools. Proficiency in Microsoft Office, particularly Excel and Word. Strong organizational skills and attention to detail, with the ability to manage multiple tasks and study activities. Excellent written and verbal communication skills. Ability to build and maintain professional relationships with investigators, coordinators, and site personnel. Strong problem-solving and analytical skills. Ability to work on-site in Texas and travel to assigned clinical trial sites as required. Recent Graduates / Entry-Level Candidates Qualified recent graduates may be considered for suitable entry-level clinical research opportunities if they have: A Master's degree in Clinical Research, Life Sciences, Pharmacy, Biotechnology, Biology, Public Health, or a related field. Relevant clinical research internship, academic research, or clinical trial experience. Understanding of GCP and clinical research fundamentals. Strong documentation, communication, analytical, and organizational skills. Familiarity with clinical research documentation, EDC systems, or clinical trial processes is an advantage. Preferred Certifications: ACRP, SOCRA, or other relevant clinical research certifications are a plus. In addition to connecting candidates with career opportunities, NextCode Placement offers separate, optional paid career-support plans for candidates who would like additional assistance with their job search. Resume optimization based on target roles $ 300/ month Resume,profile & interview Support Resume optimization based on target roles Career-support services are completely separate from the job opportunity listed above. Purchasing a career-support plan is not required to apply for this position. Candidates may apply for the position without enrolling in any paid service. Career support does guarantee interviews, not job offers, or employment. Hiring decisions are made by the respective employer based on its own requirements and selection process. #J-18808-Ljbffr
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