Feasibility Associate
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Job Summary
We are seeking a highly motivated Feasibility Associate to support our Commercial Strategy and Operations team in assessing the suitability of clinical research sites for upcoming clinical trials. This role is responsible for conducting research, maintaining global site databases, engaging with clinical research sites, and evaluating site capabilities to support study feasibility assessments.
The ideal candidate is able to work EST hours, possesses strong research and analytical skills, and has experience in clinical research, public health research, epidemiology, or related fields. A Master's Degree in Public Health (MPH) is highly preferred.
Key Responsibilities
Build, maintain, and update databases of clinical research sites globally
Communicate with research sites to assess interest and capacity for participating in clinical trials
Review study protocols, synopses, and research proposals to identify study requirements
Conduct literature reviews and online research on epidemiology, regulations, and clinical research trends
Evaluate site capabilities and research experience for proposed clinical studies
Collaborate with clinical operations teams and subject matter experts to assess site feasibility
Gather and analyze data to support site selection recommendations
Maintain accurate records and documentation within company databases and systems
Support feasibility planning activities and contribute to strategic study placement decisions
Qualifications
Bachelor's degree in Clinical Research, Public Health, Global Health, Epidemiology, Health Informatics, Life Sciences, or a related field
Master's Degree in Public Health (MPH) is highly preferred
Experience conducting research, data gathering, literature reviews, and data analysis
Experience in clinical research, public health research, epidemiology, or related research environments
Strong research, analytical, and critical-thinking skills
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
Excellent English communication skills, both written and verbal
Strong organizational skills and attention to detail
Ability to work independently and collaboratively in a global environment
Must be willing and able to work EST (Night Shift) hours
Preferred Qualifications
Experience within a Clinical Research Organization (CRO)
Experience maintaining and managing databases
Experience using Salesforce or similar CRM systems
Knowledge of clinical trial processes and site operations
Experience reviewing study protocols, synopses, or research proposals
Experience in global health, epidemiology, or healthcare research
Ability to read and understand French, Spanish, or an African language is an advantage
Why Join Us?
100% Remote Work Setup
Global Exposure in Clinical Research
Opportunity to Work with International Research Sites
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