Associate Clinical Research Manager

Role: Associate CRM oversees clinical monitoring activities and manages CRA team performance to ensure compliance with ICH-GCP, regulations, and SOPs, maintaining high-quality clinical trial execution. Objectives include resource allocation, monitoring quality assurance, and supporting site performance to meet study milestones. Responsibilities involve supervising CRA recruitment, onboarding, task assignment, performance evaluation, and mentorship; reviewing monitoring quality; supporting audits and inspections; and driving process improvements. Requirements: Bachelor's degree in a scientific or healthcare field; 5+ years industry experience in pharma, CRO, or related fields; in-depth knowledge of drug development, ICH-GCP, and trial monitoring; prior CRA experience preferred; excellent communication and organizational skills; proficiency in Microsoft Office; fluent in English. Preferred: Oncology experience. High-Value: focus on oncology trials, managing CROs and clinical teams, supporting regulatory compliance, and study milestones. Work Setup: Travel as needed; location details unspecified.