Remote Feasibility Specialist — Data & Site Insights

Worldwide Clinical Trials; United States; Remote; USD 70,000 - 90,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Feasibility Specialist to help identify and engage investigative sites for global studies. You will transform complex data into actionable insights to guide study planning and site selection.

In this remote role, you’ll collaborate with cross-functional teams, manage feasibility surveys and questionnaires, and ensure timely, high-quality deliverables. A life sciences degree and 1–2+ years in clinical research are required.

Qualifications

• Bachelor’s degree in life sciences or related field.
• 1–2+ years in clinical research, feasibility, site identification, or related field.
• Proficiency in English and strong data analysis skills.

Responsibilities

• Analyze internal and external data to identify sites and refine strategies.
• Quality-check complex site datasets to deliver reliable insights.
• Create site-facing feasibility materials aligned with study objectives.
• Design feasibility questionnaires to generate actionable site intelligence.
• Manage feasibility surveys within designated technology platforms.
• Coordinate feasibility outreach to drive site engagement and timely responses.
• Assist with Confidentiality Agreements (CDAs) when required.
• Monitor deliverables and identify risks, escalating as needed.
• Support cross-functional initiatives to improve feasibility capabilities.

Skills

Data analysis

English proficiency

Communication skills

Attention to detail

Independent work

Education

Bachelor’s degree in life sciences or related field

Tools

Word

Excel

PowerPoint

Outlook

Job description

Worldwide Clinical Trials is seeking a Feasibility Specialist to help identify and engage investigative sites for global studies. You will transform complex data into actionable insights to guide study planning and site selection.

In this remote role, you’ll collaborate with cross-functional teams, manage feasibility surveys and questionnaires, and ensure timely, high-quality deliverables. A life sciences degree and 1–2+ years in clinical research are required.