Senior Project Specialist – Real World Evidence

🔥 19 hours ago

🌵 Arizona, California, +3 more states – Remote

🌵 Arizona – Remote 🏄 California – Remote 🦞 Maine – Remote 🏈 Ohio – Remote ⚓ Rhode Island – Remote

💵 $47k - $79.9k / year

⏰ Full Time

🟠 Senior

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• 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

🏖️ Benefits

• 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