Remote Clinical Feasibility Analyst

Worldwide Clinical Trials; Oregon; Híbrido; USD 70.000 - 90.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a Feasibility Specialist to drive end-to-end site identification and data-driven feasibility activities for global studies. You will transform complex data into actionable insights and work with cross-functional teams to optimize site engagement and study planning.

Remote role open to candidates in UK, Europe and US. Strong analytical skills, English proficiency and experience in clinical research are essential, with a focus on data quality, questionnaire

Formación

• Bachelor's degree in life sciences, healthcare, business, data analytics, or a related field, or equivalent experience.
• 1-2+ years of experience in clinical research, feasibility, site identification, clinical operations, data analytics, pharmaceutical, biotechnology, or related field.
• Proficiency in English.
• Strong data analysis, data review, reconciliation, and quality-control skills.
• Ability to interpret complex information, identify discrepancies, assess risks, and communicate findings effectively.
• Excellent written and verbal communication skills with strong attention to detail and organisational abilities.
• Experience working independently, managing competing priorities, and delivering high-quality work within critical timelines.
• Proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook; experience with clinical feasibility systems, survey platforms, and investigator intelligence tools is preferred.

Responsabilidades

• Analyse internal and external data sources to develop, assess, and refine investigator and site identification strategies.
• Integrate, reconcile, interpret, and quality-check complex investigator and site datasets to deliver reliable, decision-ready insights.
• Create and maintain site-facing feasibility materials that align with protocol requirements and study objectives.
• Design and optimise feasibility questionnaires that generate actionable site intelligence and support informed study planning.
• Configure and manage feasibility surveys within designated technology platforms.
• Coordinate feasibility outreach activities, driving site engagement and ensuring high-quality, timely responses.
• Facilitate the preparation, tracking, and execution of Confidentiality Agreements (CDAs) when required.
• Monitor project deliverables and timelines, proactively identifying risks and escalating issues when appropriate.
• Contribute to cross-functional initiatives that improve feasibility capabilities, quality, efficiency, and innovation.

Conocimientos

Data analysis

Quality control

Communication

Time management

Independent work

Educación

Bachelor's degree in life sciences or related field

Herramientas

Microsoft Office

Clinical feasibility systems

Survey platforms

Investigator intelligence tools

Descripción del empleo

Worldwide Clinical Trials is seeking a Feasibility Specialist to drive end-to-end site identification and data-driven feasibility activities for global studies. You will transform complex data into actionable insights and work with cross-functional teams to optimize site engagement and study planning.

Remote role open to candidates in UK, Europe and US. Strong analytical skills, English proficiency and experience in clinical research are essential, with a focus on data quality, questionnaire