This clinical role supports global study management for Amgen's trials, coordinating planning, execution, and oversight activities from start-up through completion. The Senior Associate manages study trackers, monitors enrollment and data quality, engages sites and vendors, and escalates risks to ensure compliant, timely study delivery across multiple trial teams.
Responsibilities
Develop and maintain study trackers, dashboards, timelines, and vendor management tools
Monitor global enrollment, data flow, and quality metrics using dashboards and reports
Coordinate logistics for investigator meetings, trial events, and site communications
Manage clinical trial systems data entry and support query resolution and reconciliation
Escalate identified risks and operational issues to study team with proposed solutions
Requirements
Master's degree, or Bachelor's with 2 years clinical execution experience
Working knowledge of CTMS, eTMF, EDC systems and Microsoft Office
Proficiency in clinical trial processes and biotech/pharma/CRO environments
Strong documentation accuracy and compliance verification skills
Vendor oversight and risk-based monitoring experience
Preferred: 3 years life sciences experience including 1 year biopharmaceutical clinical research
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