Senior Project Specialist – Real World Evidence (Sponsor Dedicated /Remote -US Based)
About The Position
Syneos Health is seeking a Senior Project Specialist – Real World Evidence (RWE) to join a sponsor-dedicated team supporting innovative pharmaceutical research programs focused on real-world data and evidence generation. This role is ideal for someone who enjoys organization, coordination, problem-solving, and working behind the scenes to help complex research programs run smoothly. While this is an administrative and operational support-focused position, it is important that candidates already have exposure to the Real World Evidence (RWE) space and understand the fundamentals of how RWE studies and teams operate. This could be a great fit for someone who has supported Real World Evidence (RWE) teams, Epidemiology or observational research programs, Outcomes research initiatives, or Data Management teams within Pharmaceutical, Biotechnology, or CRO environments and is looking to continue building their career in this exciting and growing specialty area. In this role, you will support project teams responsible for both secondary data studies and primary data collection studies. You’ll 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.
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
Nice To Haves
- Experience with Late Phase and RWE projects supporting regulatory purposes, including pivotal or supportive evidence generation
- 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
Responsibilities
- Coordinating and updating study milestones and timelines
- Supporting project tracking within CTMS systems
- Scheduling and coordinating meetings
- Preparing meeting minutes and follow-up action items
- Helping teams stay organized across multiple deliverables
- Supporting operational activities for ongoing RWE studies
- Assisting with documentation, reporting, and project coordination
- Helping facilitate communication between study teams, analysts, and stakeholders
Benefits
- company car or car allowance
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
No Education Listed
