Feasibility Manager

About the company

Rovia Clinical Research is focused on advancing innovative therapies that can improve outcomes for patients and strengthen the communities it serves. The organization emphasizes a supportive, collaborative environment where employees are encouraged to grow and contribute meaningfully. Its culture is guided by five principles: People First, Humility, Integrity, One Team, and Results Accountability.

Role overview

The Feasibility Manager will be responsible for evaluating whether clinical trials can be successfully executed across a network of sites. This position involves reviewing study protocols, carrying out feasibility analyses, and partnering with internal teams to help ensure strong trial planning and delivery.

Key responsibilities

• Review historical information, site performance metrics, and patient population data to develop informed site-selection and feasibility recommendations.
• Evaluate and screen prospective research sites using study-specific factors such as patient mix, location, and investigator experience.
• Coordinate with site personnel to determine each site’s capacity, capabilities, and available resources for the proposed study.
• Perform detailed feasibility work to judge whether a site can meet expectations for recruitment, protocol adherence, and data quality.
• Assess the size and accessibility of target patient groups within each site’s catchment area, estimate recruitment timelines, and suggest ways to reduce enrollment risk.
• Analyze site-level cost factors and support budget planning, including staffing, equipment, and other required resources.
• Review local regulatory obligations and consider how they may affect site suitability and study timing.
• Partner with internal study teams, investigators, and sponsors to share feasibility findings and resolve site-specific issues.
• Prepare detailed feasibility reports and present findings to internal stakeholders with practical recommendations for study planning.
• Handle additional job-related duties as assigned.

Required skills and knowledge

This role calls for strong communication and relationship-building abilities, plus a solid understanding of clinical trial processes, regulatory expectations, medical terminology, ICH/GCP standards, FDA requirements, and HIPAA practices.

Education and experience

A bachelor’s degree is required, preferably in life sciences, health care, or a closely related discipline. Applicants should also bring at least 3 years of experience in site feasibility or study start-up within a multi-site clinical research setting.

Compensation

The salary range for this remote United States role is USD 75,000 to 90,000 per year.

Additional information

This is a full-time remote position based in the United States.