Clinical Trial Associate

Role: Clinical Trial Associate (CTA) supporting Deciphera's clinical operations team, focusing on trial execution to ensure timely, compliant, and quality-driven study delivery. Responsibilities: coordinate cross-functional study meetings, assist with site start-up and vendor management, maintain regulatory and study documentation including TMF and essential regulatory documents, support sample management and logistics, and contribute to quality assurance activities. Requirements: Bachelor’s or Master’s degree with 1-3 years in pharma, biotech, CRO, or academic research; knowledge of ICH, GCP, and global trial regulations; strong organizational skills and attention to detail. Preferred: quick learner of tools and systems, understanding of clinical data and vendor interactions, excellent communication skills, proactive team-player. High-Value: emphasis on clinical trial support within oncology or other therapeutic areas, GCP compliance, documentation management, and cross-functional collaboration. WorkSetup: details not specified, likely hybrid or onsite based on typical clinical operations roles.