Global Site Identification and Feasibility Specialist (Sponsor-Dedicated ​/ Remote US - East Coa[

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

Updated: Yesterday
Location: Remote, UT, United States
Job :-OTHLOC-1500-2

DUT-2DR

Description

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

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.

Required 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…