Clinical Research Associate

About the Role

A full-time, on-site position based in Texas, United States.

Key Responsibilities

• Monitoring clinical trial sites.
• Ensuring compliance with study protocols and adherence to applicable regulatory and ethical standards.
• Reviewing source documents and Case Report Forms (CRFs).
• Verifying data accuracy and completeness.
• Supporting site staff with clinical trial procedures.
• Documenting findings through monitoring reports.
• Collaborating with clinical operations teams.
• Supporting site initiation, routine monitoring, and closeout activities.
• Identifying and helping resolve issues affecting patient safety, protocol compliance, data integrity, or study timelines.
• Regular communication with investigators, clinical research coordinators, site personnel, and internal stakeholders.

Requirements & Tech Stack

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, Biology, or a related field.
• 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.
• 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.

Qualifications (Plus)

• Master's degree or advanced qualification in Clinical Research, Life Sciences, Pharmacy, Biotechnology, or a related discipline.
• Preferred Certifications: ACRP, SOCRA, or other relevant clinical research certifications.

Recent Graduates / Entry-Level Candidates

• 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.