Senior Project Specialist – Real World Evidence (Sponsor Dedicated /Remote -US Based)
Job Overview
Location
52 Locations
Job Type
Full-time
Category
Operations
Date Posted
May 27, 2026
Full Job Description
📋 Description
- • Support sponsor-dedicated Real World Evidence (RWE) teams in the design, coordination, and execution of secondary data studies and primary data collection studies.
- • Coordinate and update study milestones, timelines, and deliverables to ensure project progress aligns with regulatory and operational goals.
- • Maintain and update project tracking systems, including Clinical Trial Management Systems (CTMS), to ensure accurate and timely data reporting.
- • Schedule, organize, and facilitate meetings between Project Leads, epidemiologists, data analysts, and cross-functional stakeholders.
- • Prepare detailed meeting minutes and track follow-up action items to ensure accountability and timely resolution of project tasks.
- • Assist with documentation, reporting, and administrative workflows for ongoing RWE studies supporting regulatory submissions and pivotal evidence generation.
- • Facilitate communication between study teams, data management groups, and external partners to maintain alignment on project objectives and timelines.
- • Manage multiple concurrent tasks and deadlines in a fast-paced, dynamic environment while maintaining high accuracy and attention to detail.
- • Provide operational support for RWE initiatives focused on outcomes research, epidemiology, and observational studies within pharmaceutical, biotechnology, or CRO settings.
- • Collaborate with clinical operations and analytics teams to ensure seamless integration of real-world data sources into study protocols and execution plans.
- • Ensure compliance with internal processes and regulatory standards in the administration of RWE projects.
- • Contribute to continuous improvement of project coordination workflows and documentation standards within the RWE function.
- • Act as a key operational liaison between sponsor clients and internal Syneos Health teams to uphold service quality and project integrity.
- • Maintain proficiency in Microsoft Office applications to support reporting, scheduling, and data organization needs.
- • Adapt to evolving RWE methodologies and regulatory expectations to support high-impact healthcare research programs.
🎯 Requirements
- • Prior experience supporting Real World Evidence (RWE), Clinical Data Management, Epidemiology, or Observational/Outcomes Research environments
- • Experience working within Pharmaceutical, Biotechnology, or CRO settings
- • Understanding of Secondary Data Research and Primary Data Collection Studies
- • Strong organizational and coordination skills with ability to manage multiple tasks and deadlines
- • Proficiency with Microsoft Office applications
- • Experience with CTMS systems and/or clinical research operations
🏖️ Benefits
- • Health benefits including Medical, Dental, and Vision coverage
- • Company match 401(k)
- • Eligibility to participate in Employee Stock Purchase Plan
- • Eligibility to earn commissions/bonus based on company and individual performance
- • Flexible paid time off (PTO) and sick time
- • Career development and progression opportunities with technical and therapeutic area training
Skills & Technologies
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About Syneos Health, Inc.
Syneos Health is a global biopharmaceutical services organization providing clinical and commercial solutions. It integrates clinical development, outsourced commercialization, consulting, and communications services to accelerate the delivery of therapies to market. The company supports pharmaceutical, biotechnology, and medical device clients across all phases of product development and commercialization, operating in North America, Europe, and Asia-Pacific.
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