Senior Clinical Research Associate – Oncology

Role Overview

• Perform site management activities to ensure compliance with the protocol, monitoring plan, ICH GCP, local regulatory requirements, and client SOPs
• Conduct site qualification, initiation, interim, and close-out visits, both on-site and remotely
• Partner with Clinical Trial Liaison (CTL) and other client functions (e.g., Study Start-Up, Global Partnerships and Trial Optimization) to support site activation and deliverables
• Establish and maintain productive professional relationships with investigator site staff, ensuring effective communication and problem-solving throughout study conduct
• Perform drug accountability, reconciliation, and destruction, ensuring protocol compliance for storage and shipment requirements
• Prepare and maintain Oversight Monitoring Plan
• Perform review of study metrics, assess CRO Clinical Research Associate (CRA) and Investigator Site performance and identify sites for oversight monitoring visits
• Conduct Oversight Monitoring Visits at sites, either independently or alongside CRO CRA
• Review site source documentation and verify accurate data capture (ALCOA principles)
• Review and report on status of study conduct at the investigator site ensuring appropriate follow up of any identified issues/action items
• Ensure site regulatory files are current and verify timely submission of study documentation, including safety reporting
• Write and submit accurate monitoring visit reports, oversight monitoring visit reports, and study correspondence in a timely manner
• Periodically verify completeness of site documentation (e.g., investigator site file/regulatory binder contents)
• Identify and record protocol deviations, escalate non-compliance, and resolve study-related issues as necessary
• Track, trend, and report issues, escalating them to the appropriate teams when required
• Maintain ongoing communication with site personnel, study teams, CTLs, Central Monitors, and CRO CRAs
• Actively participate in team meetings and process improvement initiatives to enhance study outcomes
• Support inspection readiness activities and ensure sites maintain data integrity and protocol deliverables

Requirements

• Bachelor's degree (or equivalent)
• Minimum of 5 years of related experience for Senior CRA
• Strong analytical problem-solving skills and critical thinking abilities
• Working knowledge of the clinical drug development process, ICH GCP guidelines, and applicable regulatory requirements (e.g., FDA, EMA, PMDA)
• Effective communication and interpersonal skills to build relationships internally and externally
• Familiarity with medical terminology and proficiency in IT applications, including Microsoft Office, EDC, CTMS, and data repositories
• Demonstrated ability to deliver clear and concise written reports
• Effective prioritization and time management skills

Tech Stack

• Google Cloud Platform

Benefits

• Health insurance
• Professional development opportunities