Global Site Identification and Feasibility Specialist – Sponsor-Dedicated

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🔥 0 minutes ago

🏈 Alabama, Maine, +3 more states – Remote

🏈 Alabama – Remote 🦞 Maine – Remote 🌲 North Carolina – Remote 🏈 Ohio – Remote ⚓ Rhode Island – Remote

💵 $95k - $105k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🦅 H1B Visa Sponsor

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

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

• 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