Clinical Data Manager

Role: Clinical Data Manager at Telix Pharmaceuticals, responsible for ensuring the integrity, accuracy, and compliance of clinical trial data across global oncology and rare disease programs, including prostate cancer imaging. Responsibilities: oversee data management activities for assigned trials, including EDC development, data cleaning, documentation, vendor coordination, and supporting audits and regulatory inspections; contribute to protocol and SAP review. Requirements: Bachelor's in Health Information Management, Life Sciences, or equivalent; 3+ years in clinical trial data management with at least 1 year leading complex global trials; proficiency in EDC, CDISC standards, GCP, and regulatory compliance; experience creating data management documents and managing vendor relationships; strong organizational skills, attention to detail, and ability to work independently and collaboratively. Preferred: advanced degree. High-Value: oncology (prostate cancer), late-stage clinical trials, global scope, GCP/CDISC compliance, vendor oversight, and cross-functional collaboration. Work Setup: hybrid/remote with up to 20% travel.