Coordinate logistics for investigator meetings, trial events, and site communications.
Manage assigned start-up activities, including system setup, access management, and document readiness, ensuring completion to required standards.
Study Execution & Oversight
Use study dashboards and reports to monitor global enrollment, data flow, and quality indicators, taking proactive action to address deviations and risks.
Lead delivery of assigned risk and quality management activities
Track and report study progress, coordinating with Study team and vendors to resolve operational issues and maintain compliance.
Deliver assigned components of global recruitment and retention strategies to help ensure enrollment targets are achieved.
Manage Study Training system activities and oversight
Stakeholder Engagement & Team Collaboration
Build and maintain effective relationships with internal study team members, vendors and investigator sites
Act as a point of contact for routine study updates, ensuring stakeholders are informed and aligned.
Identify, prioritize, and escalate risks effectively to support swift, informed decisions
Site & Vendor Engagement
Lead vendors and supplier set-up to ensure quality, speed, and consistency in deliverables.
Data & Systems Management
Maintain and monitor clinical trial systems (e.g., CTMS), ensuring accurate and timely data entry and reporting.
Support data collection oversight, including query resolution and reconciliation activities.
Manage trial documentation (e.g., TMF) to ensure inspection readiness.
Process Improvement & Knowledge Sharing
Contribute to best practice development, knowledge-sharing and process improvement within the study support community.
Proactively identify and highlight opportunities to streamline / automate activities within remit.
Support Audit/Inspections including Corrective and Preventive Actions (CAPA) processes and embed lessons learned across studies.
Basic Qualifications and Experience
Master’s degree OR
Bachelor’s degree and 2 years of clinical execution experience OR
Associate’s degree and 6 years of clinical execution experience OR
High school diploma / GED and 8 years of clinical execution experience
Preferred Qualifications and Experience
3 years’ work experience in life sciences or medically related field, including 1 year of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
Experience working on global clinical trials
Competencies
Strong collaborative and effective communication skills within a team environment.
Understands importance of accuracy in documentation, data tracking, and compliance checks. Identifies discrepancies and escalates appropriately.
Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organization environments
Strong skills in using MS Word, Excel, PowerPoint, and other relevant software for documentation, data management, and trial support
Working knowledge of CTMS, eTMF, EDC, and Microsoft Office tools. Ability to maintain accurate and timely data entry. Skilled in managing clinical trial data flow, investigator documentation, and protocol adherence while ensuring regulatory compliance
Experience with overseeing vendors and suppliers
Experience executing risk-based site monitoring, Audit and Inspections Corrective and Preventive Actions (CAPA) implementation, and risk mitigation to resolve operational challenges and ensure inspection readiness
Cultural sensitivity and collaboration across global teams.
Ability to recognize, highlight and resolve issues. Demonstrates curiosity and willingness to take on new tasks.
Understanding of the clinical and pharmaceutical drug development process and clinical trial execution principles
Experience with tracking and filing of essential documents such as protocols, informed consent forms, and regulatory submissions to ensure documents are version-controlled and inspection-ready.
EQUAL OPPORTUNITY STATEMENT
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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