Senior Project Specialist – Real World Evidence

Syneos Health

Senior Project Specialist supporting innovative pharmaceutical research programs focused on real-world data at Syneos Health. Role involves project coordination and operational support within RWE environments.

Posted 7/7/2026full-timeRemote • Arizona, California, Maine, Ohio, Rhode Island • 🇺🇸 United StatesSenior💰 $47,000 - $79,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

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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.

Highest-signal resume keywords

Real World Evidence (RWE)Clinical Data ManagementCTMS SystemsEpidemiologyStrong Organizational Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Secondary Data ResearchPrimary Data CollectionProject CoordinationDocumentationReporting

Soft Skills

Strong Communication SkillsInterpersonal SkillsAbility to Manage Multiple Tasks

Tools & Technologies

Microsoft Office Applications

Industry Keywords

PharmaceuticalBiotechnologyCROObservational ResearchOutcomes Research

About the role

Key responsibilities & impact

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

What you’ll need

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

Benefits

Comp & perks

Health benefits to include Medical, Dental and Vision
Company match 401k
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