Clinical Research Associate – Neurology & Oncology

About the role

Join Worldwide Clinical Trials as a Clinical Research Associate (CRA) focused on Neurology and Oncology studies. You will work within a collaborative Clinical Operations team, supporting site activities across multiple therapeutic areas and ensuring high‑quality data collection.

Key responsibilities

• Conduct site qualification, initiation, interim monitoring, and close‑out visits.
• Mentor junior CRAs and site staff, providing guidance on protocol adherence.
• Document site visit findings and prepare written reports.
• Review safety information, informed consent, and source documents for compliance.
• Verify case report forms (CRFs) using paper or electronic data capture (EDC) systems and assist sites with query resolution.
• Maintain Trial Master File (TMF) documentation and manage investigational product (IP) accountability.
• Support regulatory submissions and provide training during accompanied site visits.

Required profile

• Strong interpersonal and communication skills.
• Ability to work independently and as part of a multidisciplinary team.
• Attention to detail and commitment to patient safety.

Required skills

• Regulatory submissions
• Trial Master File (TMF) management
• Electronic Data Capture (EDC) systems

What we offer

• Opportunity to work on cutting‑edge Neurology and Oncology trials.
• Supportive team environment with mentorship and professional development.
• Access to global CRO resources and expertise.