Senior Project Specialist – Real World Evidence Experience Required (Sponsor Dedicated /Remote -US Based)

Job Responsibilities

• Support project teams responsible for both: Secondary data studies Primary data collection studies
• Coordinating and updating study milestones and timelines
• Scheduling and coordinating meetings
• Preparing meeting minutes and follow-up action items
• Helping teams stay organized across multiple deliverables
• Assisting with documentation, reporting, and project coordination
• Helping facilitate communication between study teams, analysts, and stakeholders

Required

• Prior experience supporting work within: Real World Evidence (RWE) Clinical Data Management Epidemiology Observational or outcomes research environments
• Experience within a Pharmaceutical, Biotechnology, or CRO setting
• Understanding of: Secondary data research Primary data collection studies CTMS systems and/or clinical research operations
• Strong organizational and coordination skills
• Ability to manage multiple tasks and deadlines in a fast-paced environment
• Strong communication and interpersonal skills
• Proficiency with Microsoft Office applications
• Experience with Late Phase and RWE projects supporting regulatory purposes, including pivotal or supportive evidence generation, is considered a strong asset

Nice to Have (But Not Required)

• Experience working directly with epidemiology or data analytics teams
• Sponsor-dedicated or embedded team experience
• Exposure to healthcare databases or real-world data sources
• Life sciences or healthcare-related degree
• Interest in long-term growth within RWE, clinical operations, or healthcare analytics