Associate Clinical Project Manager
Core
Assist the Clinical Project Manager in planning, executing, and managing multiple clinical studies for oncology and other therapeutic areas.
Role type
Associate Clinical Project Manager
Builds
Clinical trials and study deliverables
Domain
Pharmaceutical / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial conduct, ICH-GCP and FDA regulations, study start-up and closeout, TMF oversight, risk mitigation, cross-functional collaboration, Microsoft Office, clinical trial systems
Preferred skills
Oncology therapeutic area knowledge, mentoring junior team members
Technologies
Microsoft Office (Word, Excel, PowerPoint, Outlook), clinical trial systems
Responsibilities
Support CPM in designing and delivering clinical studies per timelines; monitor clinical data collection; prepare and review study plans, protocols, CSRs, and regulatory submissions; coordinate clinical trial supplies; manage CRO/vendor document reviews and change orders; track invoices; prepare program updates; participate in study team and investigator meetings; update SOPs.
Seniority
Mid-level, hands-on IC
