Clinical Trials Site ICRA I — On-Site Contract Role

Medasource; Maple Grove (MN); On-site; USD 55,000 - 59,000; Full time

Job summary

Medasource seeks a Site ICRA I in Maple Grove, MN to participate in planning and execution of clinical studies at assigned sites. The role supports startup, maintenance, and close-out, ensuring compliance with study protocols and regulatory standards throughout the study lifecycle.

The position requires strong communication, organizational, and analytical skills, proficiency with Microsoft Office, and the ability to work independently.

Qualifications

• > Minimum two years of relevant experience in clinical research or related area.
• "> Strong written and verbal communication, interpersonal, presentation, analytical, and organizational skills.
• "> Ability to interpret basic clinical data and meet deadlines.

Responsibilities

• Support regulatory and clinical protocol compliance for all clinical projects at assigned sites
• Coordinate start-up, maintenance, and close out of clinical study sites in partnership with field staff and in-house personnel
• Review and analyze study data and regulatory documents for accuracy and completeness; resolve data queries and support data corrections
• Follow up and resolve findings from monitoring visits and audits at assigned study sites
• Serve as primary contact and liaison for assigned study sites, responding to protocol-related issues and escalating as appropriate
• Review informed consent documents to ensure all required elements are included
• Apply general clinical research processes and regulatory knowledge to process improvement activities
• Support training of external clinical professionals to ensure compliance with established protocols
• Perform review of site compliance under supervision and elevate issues to site operations management and/or study management
• Update and maintain internal clinical trial information and document management systems, including trial master file management
• Collect and maintain regional and site-specific communication to facilitate activation and execution of clinical studies
• Contribute to global or regional process improvements as needed
• Engage in continuing education and participate in relevant professional associations or societies related to clinical research
• Perform additional duties as assigned

Skills

Communication skills

Analytical skills

Organizational skills

MS Office proficiency

Independence

Education

Bachelor’s degree or higher in natural science or related field

SoCRA or ACRP certification preferred

Tools

Microsoft Office

Job description

Medasource seeks a Site ICRA I in Maple Grove, MN to participate in planning and execution of clinical studies at assigned sites. The role supports startup, maintenance, and close-out, ensuring compliance with study protocols and regulatory standards throughout the study lifecycle.

The position requires strong communication, organizational, and analytical skills, proficiency with Microsoft Office, and the ability to work independently.