Senior Clinical Research Associate / Clinical Research Associate II – Oncology

This is a fully remote position, open to applicants in United States.

📋 Description

• Supervision of Monitoring Duties and Study Execution

• Guarantee the proper execution of clinical trials in alignment with the Study Monitoring Plan (SMP) and relevant laws, GCP, and sponsor standards to meet project objectives, timelines, and quality standards

• Oversee specific operational elements for the execution of clinical trial activities at designated investigator sites, from site activation to database lock, ensuring that applicable timelines and quality deliverables are achieved

• Act as the main point of contact for assigned investigator sites throughout the study execution

⛳️ Requirements

• At least 3 years of relevant experience in clinical research site monitoring (preferably 2 years in Oncology) within a CRO or pharmaceutical organization

• Proficiency in English and the native language(s) of the country in which they will be working is essential

• A valid driver’s license and passport are mandatory

🏝️ Benefits

• Health insurance coverage

• Paid time off benefits

• Opportunities for professional development