[Hiring] Global Site Identification and Feasibility Specialist @Syneos Health Careers

Role Description

Global Site Identification and Feasibility Specialist (Sponsor-Dedicated / Remote US - East Coast Preferred)

Are you passionate about clinical research, data analysis, and helping bring new therapies to patients faster? We are seeking a Global Site Identification & Feasibility Specialist to join our sponsor-dedicated team and play a critical role in the successful planning and execution of global clinical trials.

In this fully remote position, you'll work closely with Development Operations teams, study start-up teams, CRO partners, and other key stakeholders to identify high-performing clinical sites, support feasibility assessments, and provide data-driven insights that influence study strategy. This is an exciting opportunity to contribute directly to rare disease and other innovative clinical development programs while working alongside a dedicated sponsor team.

Job Responsibilities

• Site Identification & Feasibility
  • Conduct research and analyze clinical data to identify and evaluate sites that best align with study requirements and enrollment goals.
  • Support feasibility activities, including:
    • Clinical system setup
    • Feasibility questionnaire development and deployment
    • Site outreach and engagement
  • Track and manage feasibility responses, ensuring timely and accurate reporting to study teams and key stakeholders.
  • Troubleshoot feasibility-related issues and provide solutions for both internally managed and outsourced studies.
• Clinical Systems & Operational Support
  • Partner with study teams to ensure accurate and complete data within Clinical Trial Management Systems (CTMS).
  • Support end users by evaluating system issues and enhancement requests and recommending solutions.
  • Generate metrics, reports, and analyses that support site selection and study planning decisions.
• Strategic Collaboration
  • Collaborate with internal teams, CROs, and external stakeholders to support global site identification and enrollment planning activities.
  • Assist with enrollment forecasting and recruitment scenario planning under the guidance of senior feasibility leaders.
  • Stay current on industry trends, regulations, and best practices related to site feasibility, patient recruitment, and trial optimization.

Qualifications

• 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.

Preferred Qualifications

• Experience with trial optimization vendors, feasibility platforms, and recruitment technologies.
• Experience supporting studies in rare disease therapeutic areas.
• Familiarity with enrollment forecasting and feasibility analytics.
• Experience working with Clinical Trial Management Systems (CTMS).

Benefits

• 100% Remote role with preference for East Coast candidates.
• Competitive salary range of $95,000 - $105,000.
• 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.