Global Site Feasibility & Data Analytics Specialist

Advanced Clinical; Wilmington (DE); On-site; USD 70,000 - 100,000; Full time

Job summary

Advanced Group is seeking a Global Site Identification and Feasibility Specialist to support clinical systems and tools used by Development Operations. You will collaborate with study teams and CROs to provide inputs, metrics, and outputs that help select suitable sites for clinical studies.

You will analyze data, identify potential sites, and assist with feasibility launches while ensuring regulatory alignment and effective communication with stakeholders.

Qualifications

• B.S. in a scientific or allied health field.
• 3+ years of clinical trial experience or 2+ years feasibility/recruitment.
• Experience with trial optimization vendors, tools, and methods.
• Excellent written and verbal communication.

Responsibilities

• Work with clinical study teams to ensure the accuracy of data in CTMS.
• Provide support to end users for issue/enhancement requests in clinical systems.
• Conduct research and data analysis to identify potential sites.
• Assist with feasibility launch including system setup and questionnaire outreach.
• Communicate with study teams and stakeholders to coordinate feasibility activities.
• Track feasibility responses and report results to internal stakeholders.
• Troubleshoot issues in the feasibility process (in-house or outsourced).
• Stay updated on regulations and trends related to site feasibility.
• Support enrollment forecasting and discuss scenarios with stakeholders.

Skills

Clinical trial conduct

Feasibility / recruitment

Analytical thinking

Data analysis

Excel

Stakeholder collaboration

Project management

Data accuracy

Time management

Regulatory awareness

Education

B.S. in scientific or allied health field

Equivalent degree

Tools

CTMS

Excel

Data analysis tools

Job description

Advanced Group is seeking a Global Site Identification and Feasibility Specialist to support clinical systems and tools used by Development Operations. You will collaborate with study teams and CROs to provide inputs, metrics, and outputs that help select suitable sites for clinical studies.

You will analyze data, identify potential sites, and assist with feasibility launches while ensuring regulatory alignment and effective communication with stakeholders.