Oncology Clinical Research Associate

3 days ago

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Parexel

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Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

Description

• Responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements. • Collaborates with the Site Manager to assure compliance with protocol and inspection readiness. • Conducts monitoring activities using different methods including both on-site and remote.

Requirements

• Previous experience performing independent monitoring visits in oncology trials is essential. • Excellent communication (verbal and written), presentation, and interpersonal skills relating to colleagues and associates, both inside and outside of the organization. • Identifies and builds effective relationships with investigator site staff and other stakeholders. • Proficiency in local language is required. • Advanced level or fluency in English is required.