Associate Clinical Research Manager

Role: Associate Clinical Research Manager overseeing clinical monitoring activities and CRA team performance within oncology trials. Primary objectives include ensuring compliance with ICH-GCP, regulations, and SOPs, maintaining quality across trials, and fostering site relationships. Responsibilities encompass resource allocation, performance management, quality assurance, risk mitigation, and supporting study milestones through site visits and audits. Leadership duties include recruiting, onboarding, task assignment, mentoring, and performance evaluations to promote team development. Requirements: Bachelor's degree or higher in a scientific/healthcare field, minimum 5 years' industry experience in pharma/CRO, strong knowledge of drug development, international standards (ICH-GCP), and trial monitoring; previous CRA experience preferred. Additional qualifications include excellent communication, organizational skills, and proficiency in Microsoft Office; fluency in English. Preferred: oncology experience, adaptability to travel, valid driver’s license. High-value biopharma specifics: oncology trials, clinical monitoring, compliance, team leadership, trial quality, site management, and regulatory adherence.