On-Site Clinical Research Associate (CRA) – Texas

Next Code Placement; Texas; Presencial; USD 85 000 - 110 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Resume optimization

Career-support plans

Resumo da oferta

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.

Qualificações

• 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.

Conhecimentos

GCP Knowledge

EDC Systems

Data Review

MS Office Excel

Site Monitoring

Communication Skills

Formação académica

Bachelor's in Life Sciences

Master's in Clinical Research

Ferramentas

CTMS

EDC Software

Descrição da oferta de emprego

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.