Global Site Identification and Feasibility Specialist – Sponsor-Dedicated
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Job Description
Global Site Identification and Feasibility Specialist supporting Syneos Health’s sponsor-dedicated clinical trials. Identifying high-performing sites and providing data-driven enrollment and study-planning insights.
Responsibilities:
- Conduct research and analyze clinical data to identify and evaluate clinical sites aligned with study requirements and enrollment goals
- Support clinical system setup, feasibility questionnaire development and deployment, and site outreach and engagement
- Track and manage feasibility responses and provide timely, accurate reporting to study teams and stakeholders
- Troubleshoot feasibility-related issues and provide solutions for internally managed and outsourced studies
- Partner with study teams to ensure accurate and complete data in Clinical Trial Management Systems
- Evaluate system issues and enhancement requests and recommend solutions to end users
- Generate metrics, reports, and analyses supporting site selection and study planning
- Collaborate with internal teams, CROs, and external stakeholders on global site identification and enrollment planning
- Assist with enrollment forecasting and recruitment scenario planning under senior feasibility leaders’ guidance
- Monitor industry trends, regulations, and best practices related to site feasibility, patient recruitment, and trial optimization
Requirements:
- Bachelor's degree in a scientific, healthcare, or related field, or equivalent experience
- 3+ years of experience with clinical trial operations and development processes, or 2+ years of experience in site feasibility, recruitment, or enrollment planning
- Strong understanding of clinical research and drug development
- Experience working with cross-functional stakeholders, CROs, and external partners
- Exceptional analytical, organizational, and problem-solving skills
- Ability to manage multiple priorities and meet challenging timelines
- Excellent written and verbal communication skills
- Advanced proficiency with Microsoft Excel and experience with data analysis and reporting
- Demonstrated project coordination or administrative experience within a sponsor, CRO, or academic research environment
- Experience with trial optimization vendors, feasibility platforms, and recruitment technologies preferred
- Experience supporting rare disease studies preferred
- Familiarity with enrollment forecasting and feasibility analytics preferred
- Experience with Clinical Trial Management Systems preferred
Benefits:
- Career development and progression
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition and total rewards program
- Company car or car allowance
- Medical, Dental and Vision health benefits
- 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)
- Sick time
- Reasonable accommodations, when appropriate
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