Site ICRA I - Clinical Trials Start-Up & Compliance

Eightelevengroup; Maple Grove (MN); On-site; USD 55,000 - 59,000; Part time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

HSA

Dependent Care FSA

401k with match

Paid time off

Sick time

Paid holidays

Employee Assistance Program

Job summary

Medasource seeks a Site ICRA I to support the planning and execution of clinical studies at the Maple Grove, MN site. This on-site contract role focuses on site activation, protocol compliance, and regulatory adherence throughout the study lifecycle.

The incumbent will collaborate with field staff and in-house teams, review consent documents, analyze data, and address findings from monitoring visits and audits. Strong communication and MS Office skills are essential.

Qualifications

• Bachelor's degree in natural science, pre-medicine, nursing, bioengineering, or related field.
• Minimum of two years of relevant experience in clinical research or related area.
• Certification as a Research Professional (SoCRA or ACRP) preferred.
• Excellent organization, coordination, accuracy, and attention to detail.
• Familiarity with clinical trials research processes.

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 with field staff and in-house personnel.
• Review and analyze study data and regulatory documents for accuracy; resolve data queries.
• Follow up and resolve findings from monitoring visits and audits at assigned study sites.
• Serve as primary contact and liaison for assigned study sites; escalate as appropriate.
• Review informed consent documents to ensure all required elements are included.
• Apply clinical research processes to process improvement activities.
• Support training of external clinical professionals to ensure protocol compliance.
• Maintain trial master file management and document systems.

Skills

Strong communication

Analytical ability

Organizational skills

MS Office proficiency

Independent work

Interpersonal skills

MS Office Suite

Education

Bachelor's degree in natural science or related field

Tools

Microsoft Office Suite

Job description

Medasource seeks a Site ICRA I to support the planning and execution of clinical studies at the Maple Grove, MN site. This on-site contract role focuses on site activation, protocol compliance, and regulatory adherence throughout the study lifecycle.

The incumbent will collaborate with field staff and in-house teams, review consent documents, analyze data, and address findings from monitoring visits and audits. Strong communication and MS Office skills are essential.