Senior Project Specialist – Real World Evidence

Stellenbeschreibung:

• Support project teams responsible for both: Secondary data studies and Primary data collection studies
• Work closely with Project Leads, epidemiologists, data analysts, Data Management teams, and cross-functional stakeholders to help keep projects organized, on track, and moving forward
• Coordinate and update study milestones and timelines
• Support project tracking within CTMS systems
• Schedule and coordinate meetings
• Prepare meeting minutes and follow-up action items
• Help teams stay organized across multiple deliverables
• Support operational activities for ongoing RWE studies
• Assist with documentation, reporting, and project coordination
• Help facilitate communication between study teams, analysts, and stakeholders

Requirements

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

Core Competencies

Demonstrates expertise in coordinating and supporting Real World Evidence (RWE) studies, including both secondary data research and primary data collection. Proficient in managing project timelines, facilitating communication among stakeholders, and utilizing CTMS systems for clinical research operations.