Lead Clinical Research Associate

📋 Description

• Oversee clinical trial activities at country/regional level with coordination and compliance.
• Provide leadership to clinical monitoring teams and ensure operational excellence.
• Monitor timelines, enrollment, data cleaning, and CAPA when needed.
• Review monitoring visit reports for quality and reporting accuracy.
• Act as main communication point between CRAs, Site Management, Project Leads, and Project Managers.
• Lead country-level project meetings, provide study updates, and escalate risks.

🎯 Requirements

• Life Sciences/Medicine/Nursing/Pharmacy or equivalent education/experience.
• Minimum 4 years of site monitoring in global clinical projects, with lead CRA experience.
• Experience monitoring US sites.
• Experience across Phase II/III monitoring visits.
• Strong knowledge of clinical trial processes, regulatory/compliance, and quality management.
• Oncology experience is strongly preferred; exposure to advanced therapies is a plus.

🎁 Benefits

• Opportunity to grow in a global clinical research environment.
• Leadership role with mentorship and strategic oversight.
• Remote study oversight and reduced travel model.
• Exposure to innovative therapeutic areas and complex programs.
• Collaborate with international teams and industry experts.
• Continuous learning and professional development support.