ZipRecruiter

Log In

2

Entry Level Clinical Research Associate Jobs in Maple Grove, MN

Medasource

Clinical Research Associate

Maple Grove, MN · On-site

Certification as a Research Professional by Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP). Work habits include organization, coordination of ...

next page

Showing results 1-20

All JobsClinical Research Associate JobsEntry Level Clinical Research Associate JobsEntry Level Clinical Research Associate Jobs in Maple Grove, MN

Entry Level Clinical Research Associate information

See Maple Grove, MN salary details

$11

$28

$59

How much do entry level clinical research associate jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for entry level clinical research associate in Maple Grove, MN is $28.61, according to ZipRecruiter salary data. Most workers in this role earn between $18.31 and $33.25 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of an entry level clinical research associate?

As an Entry Level Clinical Research Associate, your day-to-day work generally involves assisting with monitoring clinical trial sites, reviewing study documentation, and ensuring adherence to protocol and regulatory requirements. You may support more senior team members in conducting on-site or remote visits, tracking patient recruitment, and managing data collection. Additionally, you’ll communicate regularly with site staff and other stakeholders to resolve issues and ensure data quality. This hands-on experience is essential for building expertise in clinical research processes and advancing toward more senior CRA roles.

What is an entry level clinical research associate?

An Entry Level Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements, ethical guidelines, and study protocols. They assist in site selection, data collection, and verifying that study procedures are properly followed. Entry-level CRAs typically work under the supervision of senior CRAs and may travel to different clinical sites. Strong attention to detail, knowledge of Good Clinical Practice (GCP) guidelines, and organizational skills are essential. This role is a starting point for a career in clinical research, with opportunities for growth into senior CRA or project management positions.

What are the key skills and qualifications needed to thrive as an entry level clinical research associate?

To thrive as an Entry Level Clinical Research Associate, you typically need a bachelor's degree in life sciences or a related field, a solid understanding of clinical trial protocols, and attention to detail. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory documentation is often required. Strong communication, organization, and problem-solving abilities help you effectively collaborate with study sites and team members. These skills are critical to ensure the accuracy, compliance, and successful progression of clinical studies.

What job categories do people searching Entry Level Clinical Research Associate jobs in Maple Grove, MN look for?

The top searched job categories for Entry Level Clinical Research Associate jobs in Maple Grove, MN are:

What cities near Maple Grove, MN are hiring for Entry Level Clinical Research Associate jobs?

Cities near Maple Grove, MN with the most Entry Level Clinical Research Associate job openings:

Entry Level Clinical Research Associate jobs near you
Infographic showing various Entry Level Clinical Research Associate job openings in Maple Grove, MN as of August 2026, with employment types broken down into 89% Full Time, and 11% Contract. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $59,508 per year, or $28.6 per hour.

Clinical Research Associate

Medasource

Maple Grove, MN • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

Job Title: Site ICRA I

Location: Maple Grove, MN

Duration: 8-month contract (likelihood of extension)

Position Summary:

Participates in the planning and execution of Abbott clinical studies at the assigned study sites.

Supports timely site activation, compliance to study protocol, domestic and international Good Clinical

Practices, applicable regulatory standards, and Abbott Standard Operating Procedures during study

activation, execution and close out phase in close cooperation with the assigned Site Management

team. Uses existing procedures to solve routine or standard problems. Supports collection of essential

regulatory documents, obtaining missing data and data corrections, and review of protocol deviations

in cooperation with Data Review.

Essential Functions:

• Supports regulatory and clinical protocol compliance for all clinical projects at the assigned

sites.

• In partnership with the assigned Abbott field staff and in-house personnel, coordinates the start-

up, maintenance and close out of the assigned clinical study sites.

• May review informed consent documents to ensure all required elements are included.

• Reviews and analyzes study data, regulatory documents for accuracy and completeness,

supports data queries resolution.

• Supports the follow-up and resolution of findings from monitoring visits and audits on the

assigned study sites.

• Serves as a liaison to clinical study management, site management personnel and site personnel

by responding to protocol-related issues and escalating as appropriate.

• Acts as a primary contact for the assigned study sites.

• Communicates and collaborates with all levels of employees, customers, contractors, and

vendors.

• Applies general clinical research processes and regulatory knowledge to process improvement

activities.

• Supports training of external clinical professionals to ensure compliance with established

protocols.

• Performs review of site compliance under supervision and escalates issues to site operations

management and/or study management.

• Updates and maintains internal clinical trial information and document management systems

including trial master file management.

• Collect and maintain regional and study site-specific communication to facilitate activation and

execution of clinical studies at the assigned study sites.

• May contribute to global or regional process improvements.

Other Duties:

• Have a good understanding of current clinical regulations and common industry practices,

engages in relevant professional associations or societies, and seeks continuing education about

Abbott devices and therapies.

• May make additional contributions as assigned

Qualifications:

• Required: Bachelor’s degree preferably with an academic focus in natural science, pre-

medicine, nursing, bioengineering with a minimum of two years of experience, or an equivalent

combination of education and experience

• Must have strong written and verbal communication, interpersonal, presentation, analytical,

organizational skills, and the ability to interpret basic clinical data, to meet deadlines as well as

the ability to communicate effectively with all levels of employees.

• Must be proficient in Microsoft Office Suite.

• Able to work independently, seeking guidance when necessary.

• Capable of exchanging information, ask questions, and check for understanding.

Desired:

A general familiarity with clinical trials research processes. Previous related experience in research

within a clinical or corporate setting or relevant clinical experience in a clinical/hospital environment.

Certification as a Research Professional by Society of Clinical Research Associates (SoCRA) or

Association of Clinical Research Professionals (ACRP).

Work habits include organization, coordination of many tasks, accuracy, and attention to detail.

Apply