Site ICRA (Backfill)

Eight Eleven Group; 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

Site ICRA I

Maple Grove, MN

On-Site Role

$40 - $43 per hour

11-month contract (likelihood of extension)

ABOUT THE ROLE

Our client, a large medical device company, is seeking a Site ICRA I to participate in the planning and execution of clinical studies at assigned study sites in Maple Grove, MN. This role is responsible for supporting timely site activation, ensuring compliance with study protocols, domestic and international Good Clinical Practices, applicable regulatory standards, and Standard Operating Procedures throughout the study lifecycle. The Site ICRA I will collaborate closely with field staff and in-house personnel to manage study start-up, maintenance, and close-out, review informed consent documents, analyze study data, resolve data queries, and address findings from monitoring visits and audits. The position also serves as a primary contact for assigned study sites, facilitates communication, and supports process improvement activities. The role requires strong communication, organizational, and analytical skills, proficiency in Microsoft Office Suite, and the ability to work independently. Familiarity with clinical trials research processes and professional certification are considered desirable. This is an 11-month contract with the likelihood of extension.

WHAT YOU'LL DO

• 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

WHAT YOU BRING

• Bachelor's degree in natural science, pre-medicine, nursing, bioengineering, or related field (or equivalent combination of education and experience)
• Minimum of 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
• Proficiency in Microsoft Office Suite
• Ability to work independently and seek guidance when necessary
• General familiarity with clinical trials research processes
• Previous experience in clinical or corporate research or relevant clinical/hospital environment
• Certification as a Research Professional (SoCRA or ACRP) preferred
• Excellent organization, coordination, accuracy, and attention to detail
• Capable of exchanging information, asking questions, and checking for understandingEngagement in relevant professional associations or societies and commitment to continuing education

#LI-BT1

Site ICRA (Backfill) Maple Grove, MinnesotaFor over 16 years, Medasource has established and maintained relationships that are designed to meet your IT staffing needs. Whether it’s contract, contract-to-hire, or permanent placement work, we customise our search based upon your company’s unique initiatives, culture and technologies. With our national team of recruiters placed at 21 major hubs around the nation Medasource finds the people best-suited for your business. When you work with us, we work with you. That’s the Medasource promise.

Medasource is an equal opportunity employer that does not discriminate on the basis of actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, lactation and related medical conditions), gender identity or gender expression, sexual orientation, marital status, military service and veteran status, physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances.

Benefits & Perks:

Medasource offers competitive medical, dental, vision, Health Savings Account, Dependent Care FSA, and supplemental coverage with plans that can fit each employee’s needs. We offer a 401k plan that includes a company match and is fully vested after you become eligible, paid time off, sick time, and paid company holidays. We also offer an Employee Assistance Program (EAP) that provides services like virtual counseling, financial services, legal services, life coaching, etc.

Pay Disclaimer:

The pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.

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