Clinical Research Associate

Next Code Placement; Texas; Presencial; USD 85.000 - 110.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Resume optimization

Career-support plans

Descripción de la vacante

NextCode Placement seeks a Clinical Research Associate (CRA) for an on-site, full-time role in Texas. You will monitor sites, verify data, and support trial procedures with cross-functional teams.

The ideal candidate has a Life Sciences degree (Master's preferred), GCP knowledge, and experience with EDC/CTMS. Strong communication and organization are essential for timely study execution.

Formación

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, Biology or related field.
• Master's degree or advanced qualification in Clinical Research or related field is a plus.
• Hands-on CRA experience or related clinical research role.
• Strong knowledge of GCP and regulatory requirements.
• Experience with site monitoring, source data verification and data review.
• Familiarity with EDC systems and clinical trial management tools.
• Proficient in MS Office, especially Excel and Word.
• Excellent communication and organizational skills.

Responsabilidades

• Monitor clinical trial sites to ensure protocol compliance and data accuracy.
• Review source documents and CRFs for completeness and correctness.
• Support site staff with trial procedures and documentation.
• Document findings through monitoring reports and communicate with stakeholders.
• Collaborate with clinical operations on initiation, routine monitoring and closeout.
• Identify issues affecting patient safety, data integrity, or timelines and help resolve them.

Conocimientos

GCP Knowledge

EDC Systems

Data Review

MS Office Excel

Site Monitoring

Communication Skills

Educación

Bachelor's in Life Sciences

Master's in Clinical Research

Herramientas

CTMS

EDC Software

Descripción del empleo

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.